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112157-91-2

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112157-91-2 Usage

Physical state

Colorless liquid

Industry use

Commonly used in the pharmaceutical industry

Purpose

Acts as a precursor for the synthesis of various drugs and pharmaceuticals

Application

Used as a building block in organic synthesis

Chemical properties

Known for its ability to undergo a variety of chemical reactions to form complex molecules

Importance

An important intermediate in the production of pharmaceuticals like antipsychotic drugs and antidepressants

Potential

Has shown potential for use in developing new medicines

Role

Due to its versatile and important role in drug synthesis, this compound is an essential chemical in pharmaceutical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 112157-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,5 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112157-91:
(8*1)+(7*1)+(6*2)+(5*1)+(4*5)+(3*7)+(2*9)+(1*1)=92
92 % 10 = 2
So 112157-91-2 is a valid CAS Registry Number.

112157-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-aminoazepan-2-one

1.2 Other means of identification

Product number -
Other names 2H-Azepin-2-one,1-aminohexahydro

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:112157-91-2 SDS

112157-91-2Upstream product

112157-91-2Relevant articles and documents

NEW SYNTHETIC "TRICKS". FROM ALIPHATIC AMINES AND AMIDES TO AZIDES AND/OR HOW TO CONVERT RNHCOR' INTO RNHCOR" AVOIDING DRASTIC HYDROLYSES

Garcia, Jordi,Vilarrasa, Jaume

, p. 341 - 342 (2007/10/02)

Controlled reduction of N-alkyl-N-nitrosoamides to hydrazides followed by nitrosation and fragmentation affords azides in 80percent overall yields, under mild conditions.This simple idea is the basis of methods for the conversion of alkylamines and N-alkylamides to alkyl azides, of RNHCOR' into RNHCOR" or RN(COR''')2, and of lactames into ω-azido esters or ω-azido acids.

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