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676348-47-3

676348-47-3

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676348-47-3 Usage

Structure

Cyclohexanecarbonyl chloride derivative with a substituted phenyl group

Usage

Reactant in organic synthesis

Applications

Production of pharmaceuticals and agrochemicals

Reactivity

Reactive compound

Chemical reactions

Can undergo various chemical reactions to yield different products

Safety measures

Important to handle with caution and use proper safety measures due to potential reactivity and toxicity

Check Digit Verification of cas no

The CAS Registry Mumber 676348-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,3,4 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 676348-47:
(8*6)+(7*7)+(6*6)+(5*3)+(4*4)+(3*8)+(2*4)+(1*7)=203
203 % 10 = 3
So 676348-47-3 is a valid CAS Registry Number.

676348-47-3SDS

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 1-(4-methoxyphenyl)cyclohexane-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1-(4-methoxyphenyl)cyclohexanecarbonyl chloride

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:676348-47-3 SDS

676348-47-3Relevant articles and documents

AMIDE DERIVATIVES COMPRISING HETEROCYCLOALKYL RING

-

Paragraph 0346; 0347; 0350, (2020/05/20)

PROBLEM TO BE SOLVED: To provide compounds or pharmacologically acceptable salts thereof that have excellent EP300 and/or CREBBP histone acetyltransferase inhibitory activity. SOLUTION: The invention provides compounds represented by the formula (1) in the figure or pharmacologically acceptable salts thereof. (In the formula (1), ring Q1, ring Q2, ring Q3, X and L are as defined in the specification.) SELECTED DRAWING: None COPYRIGHT: (C)2020,JPO&INPIT

A mild and general one-pot preparation of cyanoethyl-protected tetrazoles

Kennedy, Lawrence J.

experimental part, p. 2010 - 2013 (2010/06/14)

Described herein is a mild and general one-pot procedure for the conversion of cyanoethyl amides to cyanoethyl-protected tetrazoles with azidotrimethylsilane via the intermediacy of imidoyl chlorides generated in situ with phosphorus pentachloride. This s

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