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921602-83-7

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921602-83-7 Usage

Chemical Structure

A derivative of cyclohexylamine with two fluorine atoms attached to the cyclohexane ring.

Usage

Commonly used in the pharmaceutical industry for the synthesis of various drug molecules.

Form

Hydrochloride salt, preferred for its stability and solubility in aqueous solutions.

Applications

Potential applications in the development of new drugs and as an intermediate in organic synthesis.

Safety

Proper safety protocols must be followed while handling and storing the compound due to its potential hazards and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 921602-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,6,0 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 921602-83:
(8*9)+(7*2)+(6*1)+(5*6)+(4*0)+(3*2)+(2*8)+(1*3)=147
147 % 10 = 7
So 921602-83-7 is a valid CAS Registry Number.

921602-83-7SDS

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 2,2-difluorocyclohexan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names 2,2-Difluorocyclohexanamine hydrochloride

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:921602-83-7 SDS

921602-83-7Relevant articles and documents

Synthesis of gem-difluorocyclopentane/hexane building blocks

Melnykov, Kostiantyn P.,Nosik, Pavel S.,Kurpil, Bohdan B.,Sibgatulin, Dmitriy A.,Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.

, p. 60 - 66 (2017/05/17)

An approach to the preparation of gem-difluorocyclopentane/hexane-derived carboxylic acids and amines is described. Whereas for 3,3-difluoro-substituted cycloalkanones, straightforward deoxofluorination of the corresponding ketoesters led to the target compounds, in the case of 2,2-difluoro isomers, the bypass or alternative routes were necessary.

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