Category: 2253-73-8

Use of Lactiplantibacillus plantarum ZJ316 as a starter culture for nitrite degradation, foodborne pathogens inhibition and microbial community modulation in pickled mustard fermentation was written by Zhang, Xiazhu;Han, Jiarun;Zheng, Xiaogu;Yan, Jiaqian;Chen, Xiaozhen;Zhou, Qingqing;Zhao, Xiaodan;Gu, Qing;Li, Ping. And the article was included in Food Chemistry: X in 2022.Quality Control of Isopropylisothiocyanate The following contents are mentioned in the article:

The potential of Lactiplantibacillus plantarum ZJ316 (ZJ316) as a starter culture for quality improvement and microbial community regulation in pickled mustard fermentation was elucidated in this study. Our results show that ZJ316 can deter the occurrence of nitrite peaks and maintain the nitrite content of pickled mustard at a low level (0.34 mg/kg). The headspace solid-phase microextraction (HS-SPME) and gas chromatog.-mass spectrometry results indicate that ZJ316 gives a good flavor to pickled mustard. According to the 16S rDNA results, Firmicutes were the predominant microbiota after inoculation with ZJ316, and the abundances of Citrobacter, Enterobacter, and Proteus decreased simultaneously. In addition, antibacterial activity anal. showed that the supernatant of pickled mustard inoculated with ZJ316 had a significant inhibitory effect on Staphylococcus aureus D48, Escherichia coli DH5α, and Listeria monocytogenes LM1. In conclusion, L. plantarum ZJ316 has potential for use as an ideal starter in the process of vegetable fermentation This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Quality Control of Isopropylisothiocyanate).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Quality Control of Isopropylisothiocyanate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Use of Lactiplantibacillus plantarum ZJ316 as a starter culture for nitrite degradation, foodborne pathogens inhibition and microbial community modulation in pickled mustard fermentation was written by Zhang, Xiazhu;Han, Jiarun;Zheng, Xiaogu;Yan, Jiaqian;Chen, Xiaozhen;Zhou, Qingqing;Zhao, Xiaodan;Gu, Qing;Li, Ping. And the article was included in Food Chemistry: X in 2022.Reference of 2253-73-8 The following contents are mentioned in the article:

The potential of Lactiplantibacillus plantarum ZJ316 (ZJ316) as a starter culture for quality improvement and microbial community regulation in pickled mustard fermentation was elucidated in this study. Our results show that ZJ316 can deter the occurrence of nitrite peaks and maintain the nitrite content of pickled mustard at a low level (0.34 mg/kg). The headspace solid-phase microextraction (HS-SPME) and gas chromatog.-mass spectrometry results indicate that ZJ316 gives a good flavor to pickled mustard. According to the 16S rDNA results, Firmicutes were the predominant microbiota after inoculation with ZJ316, and the abundances of Citrobacter, Enterobacter, and Proteus decreased simultaneously. In addition, antibacterial activity anal. showed that the supernatant of pickled mustard inoculated with ZJ316 had a significant inhibitory effect on Staphylococcus aureus D48, Escherichia coli DH5α, and Listeria monocytogenes LM1. In conclusion, L. plantarum ZJ316 has potential for use as an ideal starter in the process of vegetable fermentation This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Reference of 2253-73-8).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Reference of 2253-73-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Isothiocyanates: cholinesterase inhibiting, antioxidant, and anti-inflammatory activity was written by Burcul, Franko;Generalic Mekinic, Ivana;Radan, Mila;Rollin, Patrick;Blazevic, Ivica. And the article was included in Journal of Enzyme Inhibition and Medicinal Chemistry in 2018.Computed Properties of C4H7NS The following contents are mentioned in the article:

Finding a new type of cholinesterase inhibitor that would overcome the brain availability and pharmacokinetic parameters or hepatotoxic liability has been a focus of investigations dealing with the treatment of Alzheimer’s disease. Isothiocyanates have not been previously investigated as potential cholinesterase inhibitors. These compounds can be naturally produced from their glucosinolate precursors, secondary metabolites widely distributed in our daily Brassica vegetables. Among 11 tested compounds, Ph isothiocyanate and its derivatives showed the most promising inhibitory activity. 2-Methoxyphenyl ITC showed best inhibition on acetylcholinesterase with IC₅₀ of 0.57 mM, while 3-methoxyphenyl ITC showed the best inhibition on butyrylcholinesterase having 49.2% at 1.14 mM. Assessment of the antioxidant efficacy using different methods led to a similar conclusion. The anti-inflammatory activity was also tested using human COX-2 enzyme, ranking Ph isothiocyanate, and 3-methoxyphenyl isothiocyanate as most active, with âˆ?9% inhibition at 50 μM. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Computed Properties of C4H7NS).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Computed Properties of C4H7NS

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Enantioseparation using chitosan 2-isopropylthiourea-3,6-dicarbamate derivatives as chiral stationary phases for high-performance liquid chromatography was written by Zhang, Lili;Deng, Hongzhong;Wu, Xuepeng;Gao, Hanyuan;Shen, Jun;Cao, Huaqi;Qiao, Yingjie;Okamoto, Yoshio. And the article was included in Journal of Chromatography A in 2020.Name: Isopropylisothiocyanate The following contents are mentioned in the article:

A new class of chitosan derivatives with an isopropylthiourea at the 2-position and various carbamates at the 3,6-positions of the glucosamine skeleton was synthesized by the selective thiocarbamoylation of the 2-amino group. The chiral stationary phases (CSPs) were then prepared by coating the obtained chitosan 2-isopropylthiourea-3,6-dicarbamate derivatives onto silica gel. The enantioseparation property of the chitosan-based CSPs was assessed with twelve racemates by high-performance liquid chromatog. (HPLC). The CSPs displayed a characteristic enantioseparation power, which seemed to be significantly affected by the 3,6-substituents of the glucosamine unit. The chitosan derivatives with the 3,6-diphenylcarbamate, except for 2-methylphenylcarbamate, possessed higher enantioseparation abilities than those with the 3,6-dicyclohexylcarbamate. Compared to other chitosan derivatives with 2-various substituents and commercialized Chiralcel OD, the chitosan 2-isopropylthiourea derivatives revealed a relatively higher enantioselectivity for some racemic compounds This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Name: Isopropylisothiocyanate).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Name: Isopropylisothiocyanate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Enantioseparation using chitosan 2-isopropylthiourea-3,6-dicarbamate derivatives as chiral stationary phases for high-performance liquid chromatography was written by Zhang, Lili;Deng, Hongzhong;Wu, Xuepeng;Gao, Hanyuan;Shen, Jun;Cao, Huaqi;Qiao, Yingjie;Okamoto, Yoshio. And the article was included in Journal of Chromatography A in 2020.Formula: C4H7NS The following contents are mentioned in the article:

A new class of chitosan derivatives with an isopropylthiourea at the 2-position and various carbamates at the 3,6-positions of the glucosamine skeleton was synthesized by the selective thiocarbamoylation of the 2-amino group. The chiral stationary phases (CSPs) were then prepared by coating the obtained chitosan 2-isopropylthiourea-3,6-dicarbamate derivatives onto silica gel. The enantioseparation property of the chitosan-based CSPs was assessed with twelve racemates by high-performance liquid chromatog. (HPLC). The CSPs displayed a characteristic enantioseparation power, which seemed to be significantly affected by the 3,6-substituents of the glucosamine unit. The chitosan derivatives with the 3,6-diphenylcarbamate, except for 2-methylphenylcarbamate, possessed higher enantioseparation abilities than those with the 3,6-dicyclohexylcarbamate. Compared to other chitosan derivatives with 2-various substituents and commercialized Chiralcel OD, the chitosan 2-isopropylthiourea derivatives revealed a relatively higher enantioselectivity for some racemic compounds This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Formula: C4H7NS).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Formula: C4H7NS

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Regioselective (thio)carbamoylation of 2,7-di-tert-butylpyrene at the 1-position with iso(thio)cyanates was written by Wrona-Piotrowicz, Anna;Witalewska, Marzena;Zakrzewski, Janusz;Makal, Anna. And the article was included in Beilstein Journal of Organic Chemistry in 2017.Formula: C4H7NS The following contents are mentioned in the article:

It has been found that 2,7-di-tert-butylpyrene reacts with aliphatic iso(thio)cyanates X=C=NR (R = Et, Bu, cyclohexyl, etc.) in the presence of trifluoromethanesulfonic acid to exclusively afford the corresponding 1-substituted (thio)amides I (R¹ = H, C(O)NHC₆H₅, C(S)NHC₆H₅, C(S)NHCH₂C₆H₅, 4-CH₃OC₆H₄NHC(O); R² = H; X = O, S) in high yields. For aromatic iso(thio)cyanates X=C=NR (R = Ph, benzyl and 4-methoxyphenyl) the reaction is less regioselective, although substitution at the 1-position prevails. For ethoxycarbonyl isothiocyanate, apart from the 1-substituted thioamide I (R = C(O)OC₂H₅; R¹ = H; R² = H; X = S), 1,8-disubstituted thioamide I (R = C(O)OC₂H₅; R¹ = H; R² = C(S)NHC(O)OC₂H₅; X = S) and 2,7-di-tert-butylpyrene-1-carbonitrile are formed (especially at longer reaction times). This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Formula: C4H7NS).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Formula: C4H7NS

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Novel thiosemicarbazone derivatives containing benzimidazole moiety: Green synthesis and anti-malarial activity was written by Divatia, Saavani M.;Rajani, Dhanji P.;Rajani, Smita D.;Patel, Hitesh D.. And the article was included in Arabian Journal of Chemistry in 2019.Category: esters-buliding-blocks The following contents are mentioned in the article:

A series of (E)-2-[5-chloro-1-(1H-benzo[d]imidazol-2-yl)ethylidene]-N-(substituted)hydrazine carbothioamides and (E)-2-[1-(1H-benzo[d]imidazol-2-yl)ethylidene]-N-(substituted)hydrazine carbothioamides I (X = H, Cl; R = H, Ph, Et, etc.) were prepared via the synthesis of 1-(substituted-1H-benzimidazol-2-yl)ethanol which was synthesized by the condensation of substituted o-phenylenediamine with DL-lactic acid followed by oxidation with sodium hypochlorite in mild acidic condition to form the corresponding ketones. Final compounds were formed by condensation of corresponding ketones with different thiosemicarbazides. A total of 40 compounds were synthesized and evaluated for anti-malarial properties. Among the compounds tested I (X = Cl, H; R = OCC₆H₅, 4-FC₆H4, 4-IC₆H₄, 4-MeC₆H₄, 2,3-Cl₂C₆H₃, 3,4-ClC₆H₃, c-C₆H₁₁, 4-MeOC₆H₄) exhibited good antimalarial activity in vitro. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Category: esters-buliding-blocks).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Category: esters-buliding-blocks

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Novel thiosemicarbazone derivatives containing benzimidazole moiety: Green synthesis and anti-malarial activity was written by Divatia, Saavani M.;Rajani, Dhanji P.;Rajani, Smita D.;Patel, Hitesh D.. And the article was included in Arabian Journal of Chemistry in 2019.Computed Properties of C4H7NS The following contents are mentioned in the article:

A series of (E)-2-[5-chloro-1-(1H-benzo[d]imidazol-2-yl)ethylidene]-N-(substituted)hydrazine carbothioamides and (E)-2-[1-(1H-benzo[d]imidazol-2-yl)ethylidene]-N-(substituted)hydrazine carbothioamides I (X = H, Cl; R = H, Ph, Et, etc.) were prepared via the synthesis of 1-(substituted-1H-benzimidazol-2-yl)ethanol which was synthesized by the condensation of substituted o-phenylenediamine with DL-lactic acid followed by oxidation with sodium hypochlorite in mild acidic condition to form the corresponding ketones. Final compounds were formed by condensation of corresponding ketones with different thiosemicarbazides. A total of 40 compounds were synthesized and evaluated for anti-malarial properties. Among the compounds tested I (X = Cl, H; R = OCC₆H₅, 4-FC₆H4, 4-IC₆H₄, 4-MeC₆H₄, 2,3-Cl₂C₆H₃, 3,4-ClC₆H₃, c-C₆H₁₁, 4-MeOC₆H₄) exhibited good antimalarial activity in vitro. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Computed Properties of C4H7NS).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Computed Properties of C4H7NS

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Synthesis, Antifungal Activity and 3D-QSAR Study of Novel Anisaldehyde-Derived Amide-Thiourea Compounds was written by Li, Rong;Cen, Bo;Duan, Wengui;Lin, Guishan. And the article was included in Chemistry & Biodiversity in 2022.Product Details of 2253-73-8 The following contents are mentioned in the article:

Succinate dehydrogenase (SDH) is an important target enzyme for designing agricultural chem. fungicides. In order to explore novel natural product-based antifungal agents, twenty-one unreported anisaldehyde-derived amide-thiourea compounds I (R = Me, cyclohexyl, Ph, etc.) were designed and synthesized using the principle of active splicing, and structurally confirmed. In vitro antifungal activity of the target compounds was evaluated by the agar dilution method. The results showed that some target compounds exhibited better or comparable antifungal activity than that of the com. fungicide chlorothalonil, in which compounds I (R = 3-nitrophenyl, 4-chlorophenyl, Me) displayed excellent antifungal activity of 92.6%, 92.6% and 99.1% against P. piricola, resp., better than that of the pos. control. In addition, 3D-QSAR anal. was carried out by the CoMFA method to reveal the relationship between the structures of the target compounds and their inhibitory activities. The simulative binding mode of the target compounds and SDH was also studied by mol. docking. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Product Details of 2253-73-8).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Product Details of 2253-73-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Synthesis, Antifungal Activity and 3D-QSAR Study of Novel Anisaldehyde-Derived Amide-Thiourea Compounds was written by Li, Rong;Cen, Bo;Duan, Wengui;Lin, Guishan. And the article was included in Chemistry & Biodiversity in 2022.Related Products of 2253-73-8 The following contents are mentioned in the article:

Succinate dehydrogenase (SDH) is an important target enzyme for designing agricultural chem. fungicides. In order to explore novel natural product-based antifungal agents, twenty-one unreported anisaldehyde-derived amide-thiourea compounds I (R = Me, cyclohexyl, Ph, etc.) were designed and synthesized using the principle of active splicing, and structurally confirmed. In vitro antifungal activity of the target compounds was evaluated by the agar dilution method. The results showed that some target compounds exhibited better or comparable antifungal activity than that of the com. fungicide chlorothalonil, in which compounds I (R = 3-nitrophenyl, 4-chlorophenyl, Me) displayed excellent antifungal activity of 92.6%, 92.6% and 99.1% against P. piricola, resp., better than that of the pos. control. In addition, 3D-QSAR anal. was carried out by the CoMFA method to reveal the relationship between the structures of the target compounds and their inhibitory activities. The simulative binding mode of the target compounds and SDH was also studied by mol. docking. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Related Products of 2253-73-8).

Isopropylisothiocyanate (cas: 2253-73-8) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Related Products of 2253-73-8

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics