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17343-54-3

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17343-54-3 Usage

General Description

(S)-benzyl 1-cyanoethylcarbaMate is a chemical compound with the molecular formula C17H18N2O2. It is a derivative of carbamic acid and is produced by reacting (S)-benzyl 1-aminoethylcarbaMate and cyanogen bromide. (S)-benzyl 1-cyanoethylcarbaMate is widely used in organic synthesis as a building block for various pharmaceuticals and agrochemicals. Its unique structure and reactivity make it a valuable tool for the development of new materials and chemical processes. Additionally, (S)-benzyl 1-cyanoethylcarbaMate has potential applications in the production of chiral drugs and as a starting material for the synthesis of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 17343-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,4 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17343-54:
(7*1)+(6*7)+(5*3)+(4*4)+(3*3)+(2*5)+(1*4)=103
103 % 10 = 3
So 17343-54-3 is a valid CAS Registry Number.

17343-54-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-(benzyloxycarbonylamino)-propionitrile

1.2 Other means of identification

Product number -
Other names BENZYL N-[(1S)-1-CYANOETHYL]CARBAMATE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17343-54-3 SDS

17343-54-3Relevant articles and documents

Dehydration of Chiral α-Amides to Chiral α-Nitriles Under the Appel Reaction Conditions

Shekharappa,Roopesh Kumar,Srinivasulu,Sureshbabu, Vommina V.

, p. 497 - 502 (2020/07/30)

An efficient synthesis of Nα-protected amino nitriles from Nα-protected amino acid amides employing Ph3P, I2 and NMM was described. Various amino acid amides, protected by Fmoc, Z and Boc were conveniently conve

ANTIBACTERIAL COMPOUND AND USES OF SAME

-

, (2020/09/15)

A new compound exhibiting particularly advantageous antibacterial properties, and having the structural formula: L-pyroglutamyl-L-1-aminoethyltetrazole (or N-(1-(1H-tetrazol-5-yl)ethyl)-5-oxopyrrolidine-2-carboxamide). Also, the use of this compound in mi

CATHEPSIN CYSTEINE PROTEASE INHIBITORS

-

Page/Page column 57, (2015/04/28)

This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis.

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