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81539-57-3

2-CHLORO-1-(4-HEXYL-PHENYL)-ETHANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81539-57-3

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81539-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81539-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,3 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81539-57:
(7*8)+(6*1)+(5*5)+(4*3)+(3*9)+(2*5)+(1*7)=143
143 % 10 = 3
So 81539-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H19ClO/c1-2-3-4-5-6-12-7-9-13(10-8-12)14(16)11-15/h7-10H,2-6,11H2,1H3

81539-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(4-hexylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-Chloro-1-(4-hexyl-phenyl)-ethanone

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:81539-57-3 SDS

81539-57-3Relevant articles and documents

Inhibitors of the interaction of a thyroid hormone receptor and coactivators: Preliminary structure-activity relationships

Arnold, Leggy A.,Kosinski, Aaron,Estébanez-Perpi?á, Eva,Fletterick, Robert J.,Guy, R. Kiplin

, p. 5269 - 5280 (2008/03/12)

The modulation of gene regulation by blocking the interaction between the thyroid receptor (TR) and obligate coregulators has been reported recently with the discovery of the lead compound 3-(dimethylamino)-1-(4-hexylphenyl)propan-1- one). Herein we repor

Synthesis of 1,2-diamino imidazole derivatives by the reaction of benzaldehyde guanylhydrazone with α-haloalkyl aryl ketones

Ivashchenko,Lazareva,Prudnikova,Ivashchenko,Rumyantsev

, p. 185 - 189 (2007/10/02)

2-Amino-1-benzylideneamino-4-arylimidazoles were obtained by the reaction of benzaldehyde guanylhydrazone with 4-alkyl- and 4-aryl-Ω-haloacetophenones. Side products of this reaction were cis- and trans-1,1′-bis(benzylideneamino)-4,4′-diaryl-2,2′-azoimida

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