Tag: 100-200

Synthesis and preliminary data on new selective and potent gastric prokinetic substituted benzamides was written by Del Corona, L.;Signorelli, G.;Pinzetta, A.;Coppi, G.. And the article was included in European Journal of Medicinal Chemistry in 1993.Application In Synthesis of Methyl 5-amino-4-fluoro-2-methoxybenzoate The following contents are mentioned in the article:

A series of amino-halogen-N-[2-aminoethyl] benzamides, e.g., I, was synthesized and evaluated for enhancing gastric emptying. Compared to metoclopramide, domperidone and bromopride, a number of compounds were more active in enhancing gastric motility (rat stomach emptying), devoid of dopaminergic D₂-receptor antagonism (rat apomorphine test) and were less toxic. This study involved multiple reactions and reactants, such as Methyl 5-amino-4-fluoro-2-methoxybenzoate (cas: 151793-18-9Application In Synthesis of Methyl 5-amino-4-fluoro-2-methoxybenzoate).

Methyl 5-amino-4-fluoro-2-methoxybenzoate (cas: 151793-18-9) 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.Application In Synthesis of Methyl 5-amino-4-fluoro-2-methoxybenzoate

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

Head-space-GC MS determination of volatile organic compounds in filmed paint was written by Ma, Teng-zhou;Wu, Xiao-hong;Mao, Ye-hui;Zhou, Hui;Shen, Bo;Wang, Min-hua;Sun, Ming-xing. And the article was included in Fudan Xuebao, Ziran Kexueban in 2013.Computed Properties of C7H14O3 The following contents are mentioned in the article:

Seven volatile organic compounds (VOC’s) such as toluene, xylene, ethylbenzene, hexamethyl ethanone, Et 3-ethoxypropionate 6-methyl-2-heptanone, and benzyl alc. in filmed paint were determined by head-space gas chromatog. mass spectrometry using matrix matching calibration to compensate the matrix interference. This method is simplify, good reproducibility, high sensitivity, accuracy and reliability of qual. and quant. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Computed Properties of C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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, including apples, durians, pears, bananas, pineapples, and strawberries. 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 C7H14O3

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

Heck reactions catalyzed by Pd(0)-PVP nanoparticles under conventional and microwave heating was written by Martins, Daniela de L.;Alvarez, Heiddy M.;Aguiar, Lucia C. S.;Antunes, Octavio A. C.. And the article was included in Applied Catalysis, A: General in 2011.Product Details of 763-69-9 The following contents are mentioned in the article:

Pd(0) nanoparticles stabilized by polyvinylpyrrolidone (Pd-PVP) with a diameter of 3-6 nm in ethanol catalyzed Heck coupling of iodobenzene with different alkenes under microwave heating. Products were obtained in good yields (62-99%) and good selectivity to the E-isomers. Microwave heating proved to be superior to conventional heating, providing products in higher yields and selectivities in short times (12 min). This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Product Details of 763-69-9).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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 are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Product Details of 763-69-9

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

Three-component bis-heterocyclization for synthesis of 2-aminobenzo[4,5]thieno[3,2-d]thiazoles was written by Huang, Huawen;Qu, Zhonghua;Ji, Xiaochen;Deng, Guo-Jun. And the article was included in Organic Chemistry Frontiers in 2019.Application of 2253-73-8 The following contents are mentioned in the article:

A cooperative base system has been developed for the novel three component bis-heterocyclization of methylketoxime acetates. The present protocol provides an effective entry to 2-aminobenzo[4,5]thieno[3,2-d]thiazoles, e.g., I. Mechanistically, the formation of trisulfur radical anion [S₃] ̇^– and Willgerodt-Kindler-type sulfuration would be the key for this transformation. This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Application 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. Polyesters are important plastics, with monomers linked by ester moieties. 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.Application of 2253-73-8

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

Power Law Expressions for Predicting Lower and Upper Flammability Limit Temperatures was written by Mathieu, Didier. And the article was included in Industrial & Engineering Chemistry Research in 2013.Computed Properties of C7H14O3 The following contents are mentioned in the article:

By analogy with recent models for flash point, the lower and upper flammability limit temperatures of organic compounds are represented as power law expressions in terms of fragment contributions. The predictive value of the resulting models compares well with recently published methods. A major advantage of the present approach is the fact it provides better insight into the relations between flammability limit temperatures and mol. structure. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9Computed Properties of C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Computed Properties of C7H14O3

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

Prediction of upper flammability limit percent of pure compounds from their molecular structures was written by Gharagheizi, Farhad. And the article was included in Journal of Hazardous Materials in 2009.COA of Formula: C7H14O3 The following contents are mentioned in the article:

In this study, a quant. structure-property relationship (QSPR) is presented to predict the upper flammability limit percent (UFLP) of pure compounds The obtained model is a five parameters multi-linear equation. The parameters of the model are calculated only from chem. structure. The average absolute error and squared correlation coefficient of the obtained model over all 865 pure compounds used to develop the model are 9.7%, and 0.92, resp. This study involved multiple reactions and reactants, such as Ethyl 3-ethoxypropanoate (cas: 763-69-9COA of Formula: C7H14O3).

Ethyl 3-ethoxypropanoate (cas: 763-69-9) 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.COA of Formula: C7H14O3

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

Microwave-Assisted Rapid Regioselective One-Pot Synthesis of Novel 2-Oxothiazolidine Dicarboxylate was written by Bangade, Vikas Madhukar;Mali, Prakash Rambhau;Shirsat, Prashishkumar Kishan;Meshram, Harshadas Mitaram. And the article was included in ChemistrySelect in 2019.Quality Control of Isopropylisothiocyanate The following contents are mentioned in the article:

A regioselective synthesis of 2-oxothiazolidine dicarboxylate (OTDC) under microwave irradiations is reported. Methoxylation, demethylation and double reductive cyclization occurs in single step by three component one pot reaction under microwave irradiations. The microwave irradiations, planar arrangement of intermediate imino(sp²)-thio-maleate and in situ demethylation considered as driving forces for regioselective cyclization. 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 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. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Quality Control of Isopropylisothiocyanate

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

Characteristics of selected alcoholic beverages was written by Dworska, Anna;Zalewska, Teresa;Kuprys, Marta P.;Stecka, Krystyna M.;Przegonski, Krzysztof. And the article was included in Postepy Nauki i Technologii Przemyslu Rolno-Spozywczego in 2011.COA of Formula: C9H16O4 The following contents are mentioned in the article:

The composition of infusion type alc. beverages (tinctures) made from ethanol, sugar, pine shoots, and fruits (sour cherry, nuts, raspberry) was examined with emphasis on the contents of ethanol, HCN, polyphenols, phenolic acids, flavonoids, vitamins B₁, B₂ and C, antioxidants (DPPH and ABTS assays), and volatile flavor compounds The relation between specific flavor compounds and the beverage type were also evaluated. This study involved multiple reactions and reactants, such as Ethyl methyl adipate (cas: 18891-13-9COA of Formula: C9H16O4).

Ethyl methyl adipate (cas: 18891-13-9) 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.COA of Formula: C9H16O4

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

A New Protocol for Catalytic Reduction of Alkyl Chlorides Using an Iridium/Bis(benzimidazol-2′-yl)pyridine Catalyst and Triethylsilane was written by Fukuyama, Takahide;Hamada, Yuki;Ryu, Ilhyong. And the article was included in Synthesis in 2021.Application of 112-14-1 The following contents are mentioned in the article:

The reduction of alkyl/aryl chlorides RX (R = n-dodecyl, adamantan-1-yl, naphthalen-1-yl, etc.) using triethylsilane is investigated. Primary, secondary, tertiary, and benzylic C-Cl bonds were effectively converted into C-H bonds using [IrCl(cod)]₂/2,6-bis(benzimidazol-2-yl)pyridine catalyst system. This catalyst system is quite simple since the tridentate N-ligand can be easily prepared in one step from com. available reagents. This study involved multiple reactions and reactants, such as Octyl acetate (cas: 112-14-1Application of 112-14-1).

Octyl acetate (cas: 112-14-1) 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. 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. Application of 112-14-1

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

Iron-catalyzed oxidative functionalization of C(sp³)-H bonds under bromide-synergized mild conditions was written by Yu, Han;Zhao, Qixin;Wei, Zheyu;Wu, Zhikang;Li, Qi;Han, Sheng;Wei, Yongge. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2019.Computed Properties of C8H16O2 The following contents are mentioned in the article:

An efficient oxidation and functionalization of C-H bonds with an inorganic-ligand supported iron catalyst and hydrogen peroxide to prepare the corresponding ketones, e.g., 9H-fluoren-9-one was achieved using the bromide ion as a promoter. Preliminary mechanistic investigations indicated that the bromide ion can bind to FeMo₆ to form a supramol. species (FeMo₆.2Br), which can effectively catalyze the reaction. This study involved multiple reactions and reactants, such as Methyl heptanoate (cas: 106-73-0Computed Properties of C8H16O2).

Methyl heptanoate (cas: 106-73-0) 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 are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Computed Properties of C8H16O2

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