127536-31-6 Usage
Description
benzyl carbamate is a versatile carbamate derivative featuring a N-(1-Cyano-1-phenyl)methyl group attached to a benzyl group. This chemical compound is widely recognized for its utility in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its structural properties allow it to serve as a protecting group for amines and contribute to the preparation of carbamate-based enzyme inhibitors. Furthermore, it finds applications in the production of polyurethanes and as a curing agent for epoxy resins, showcasing its broad relevance in the chemical industry.
Uses
Used in Pharmaceutical Synthesis:
benzyl carbamate is used as a reagent for the synthesis of various pharmaceuticals, facilitating the creation of new medications and contributing to advancements in healthcare.
Used in Agrochemical Production:
In the agrochemical industry, benzyl carbamate is utilized as a reagent in the production of compounds that serve to protect crops and enhance agricultural productivity.
Used as a Protecting Group for Amines:
benzyl carbamate is employed as a protecting group for amines during chemical reactions, ensuring the selective protection and deprotection of amine functional groups, which is crucial for the synthesis of complex organic molecules.
Used in Enzyme Inhibition:
This carbamate derivative is used in the preparation of carbamate-based inhibitors of enzymes, playing a significant role in the development of drugs that target specific enzymes involved in various diseases.
Used in Polyurethane Production:
benzyl carbamate contributes to the production of polyurethanes, a class of polymers with diverse applications, including flexible and rigid foams, adhesives, coatings, elastomers, and fibers.
Used as a Curing Agent for Epoxy Resins:
In the field of materials science, benzyl carbamate is used as a curing agent for epoxy resins, enhancing the properties of the final product and expanding its potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 127536-31-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,3 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 127536-31:
(8*1)+(7*2)+(6*7)+(5*5)+(4*3)+(3*6)+(2*3)+(1*1)=126
126 % 10 = 6
So 127536-31-6 is a valid CAS Registry Number.
127536-31-6Relevant articles and documents
Conversion of N-benzyloxycarbonylamino- and N-Tosylamino-benzyl phenylsulfones by green Strecker reactions to α-aminobenzyl nitriles using potassium hexacyanoferrate(II)
Hu, Xiaochun,Li, Rongzhi,Li, Zheng
, p. 432 - 436 (2014/08/05)
The cyanation of aldimines, generated in situ from N- benzyloxycarbonylamino- and N-tosylamino-benzyl phenylsulfones, to the corresponding N-protected a-aminobenzyl nitriles has been achieved by eco-friendly Strecker reactions using potassium hexacyanofer
A mild and efficient catalytic Strecker reaction of N-alkoxycarbonylamino sulfones with trimethylsilyl cyanide using indium(III) chloride: A facile synthesis of α-aminonitriles
Das, Biswanath,Damodar, Kongara,Shashikanth, Boddu,Srinivas, Yallamalla,Kalavathi, Itikala
experimental part, p. 3133 - 3136 (2009/06/17)
The Strecker reaction of N-alkoxycarbonylamino sulfones with trimethylsilyl cyanide in the presence of catalytic amount of indium(III) chloride at room temperature produces the corresponding protected α;-aminonitriles in high yields. Georg Thieme Verlag Stuttgart.
A NEW SYNTHESIS OF AN AMINO ACID BASED SWEETENER
Katritzky, Alan R.,Shobana, N.,Harris, Philip A.
, p. 121 - 126 (2007/10/03)
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