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2,4-Cyclohexadien-1-one, 6-[3-[4-(2-chloroethyl)phenyl]-1-hydroxy-2-oxohexylidene]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62018-13-7

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62018-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62018-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,1 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62018-13:
(7*6)+(6*2)+(5*0)+(4*1)+(3*8)+(2*1)+(1*3)=87
87 % 10 = 7
So 62018-13-7 is a valid CAS Registry Number.

62018-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[3-[4-(2-Chloro-ethyl)-phenyl]-1-hydroxy-2-oxo-hex-(Z)-ylidene]-cyclohexa-2,4-dienone

1.2 Other means of identification

Product number -
Other names -

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:62018-13-7 SDS

62018-13-7Upstream product

62018-13-7Downstream Products

62018-13-7Relevant academic research and scientific papers

In vitro metabolism of a new 4 hydroxycoumarin anticoagulant. Structure of an unusual metabolite

Thonnart,Vanhaelen,Vanhaelen Fastre

, p. 604 - 606 (1977)

The metabolism of clocoumarol, 3-[1-[p-(2-chlorethyl)phenyl]butyl]-4-hydroxycoumarin, by rat liver microsomes was investigated. The chemical structure of the main metabolite is 6-[1-hydroxy-2-oxo-3-[p-(2-chloroethyl)-phenyl]hexylidene]-2,4 cyclohexadien-1-one; such a structure has not been previuously reported for metabolites from anticoagulants of the 4-hydroxycoumarin group.

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