127536-31-6

Basic information

• Product Name: benzyl carbamate
• Synonyms: benzyl carbamate
• CAS NO: 127536-31-6
• Molecular Weight: 266.299
• Mol File: 127536-31-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: benzyl carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl carbamate(127536-31-6)
• EPA Substance Registry System: benzyl carbamate(127536-31-6)

Safety Data

• Hazardous Substances Data: 127536-31-6(Hazardous Substances Data)

Usage

General Description

benzyl carbamate is a chemical compound that is commonly used as a reagent in various chemical reactions. It is a carbamate derivative with a N-(1-Cyano-1-phenyl)methyl group attached to a benzyl group. benzyl carbamate is often utilized in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is known for its ability to act as a protecting group for amines, as well as its use in the preparation of carbamate-based inhibitors of enzymes. Additionally, it can also be employed in the production of polyurethanes and as a curing agent for epoxy resins. Overall, benzyl carbamate has a wide range of applications in the chemical industry.

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 613-90-1 benzoyl cyanide 
• 383366-27-6 benzyl phenyl(phenylsulfonyl)methylcarbamate 
• 372199-85-4 [phenyl-(toluene-4-sulfonyl)-methyl]-carbamic acid benzyl ester 
• 125453-15-8 benzyl carbamate 
• 151-50-8 potassium cyanide 
• 501-53-1 benzyl chloroformate 
• 16750-42-8 2-amino-2-phenylacetonitrile 

Downstream Products

• 125515-95-9 benzyl (2-amino-2-oxo-1-phenylethyl)carbamate 

Relevant articles and documents

Conversion of N-benzyloxycarbonylamino- and N-Tosylamino-benzyl phenylsulfones by green Strecker reactions to α-aminobenzyl nitriles using potassium hexacyanoferrate(II)

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

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

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