Tarasova, Olga A. et al. published their research in Synthesis in 2019 | CAS: 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, including apples, durians, pears, bananas, pineapples, and strawberries. 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.Safety of Isopropylisothiocyanate

Synthesis of 2-[(5-Amino-1H-pyrrol-2-yl)sulfanyl]acetic Acid Esters: One-Pot Assembly from Propargyl Amines, Isothiocyanates, and Alkyl 2-Bromoacetates was written by Tarasova, Olga A.;Nedolya, Nina A.;Albanov, Alexander I.;Trofimov, Boris A.. And the article was included in Synthesis in 2019.Safety of Isopropylisothiocyanate The following contents are mentioned in the article:

The compounds 2-[(5-Amino-1 H-pyrrol-2-yl)sulfanyl]acetic acid esters I (R = R1 = Me, Et, Pr; RR1 = -(CH2)4-, -(CH2)5-, -(CH2)2O(CH2)2-; R2 = Me, Et, i-Pr, n-Bu, CH2CH2OCH=CH2; R3 = Me, Et, i-Pr, t-Bu, Bn) have been synthesized in up to 77% yield by the one-pot reaction of lithiated propargylamines RR1NCH2CCH with isothiocyanates R2N=C=S followed by sequential treatment with t-BuOK-DMSO and alkyl 2-bromoacetates BrCH2CO2R3. The process occurs through the initial formation of the thiophene core, followed by its recyclization into the pyrrole nucleus at a higher temperature (ca. 45-60 °C). This study involved multiple reactions and reactants, such as Isopropylisothiocyanate (cas: 2253-73-8Safety 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, including apples, durians, pears, bananas, pineapples, and strawberries. 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.Safety of Isopropylisothiocyanate

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