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21060-31-1

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21060-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21060-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21060-31:
(7*2)+(6*1)+(5*0)+(4*6)+(3*0)+(2*3)+(1*1)=51
51 % 10 = 1
So 21060-31-1 is a valid CAS Registry Number.

21060-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1-(4-Phenylcyclohexyl)-1-ethanon

1.2 Other means of identification

Product number -
Other names trans-1-acetil-4-fenilcicloesano

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:21060-31-1 SDS

21060-31-1Relevant articles and documents

Discovery of functionalized bisimidazoles bearing cyclic aliphatic-phenyl motifs as HCV NS5A inhibitors

Zhong, Min,Peng, Eric,Huang, Ningwu,Huang, Qi,Huq, Anja,Lau, Meiyen,Colonno, Richard,Li, Leping

, p. 5731 - 5737 (2015/01/08)

This Letter describes the discovery of a number of functionalized bisimidazoles bearing a cyclohexylphenyl, piperidylphenyl, or bicyclo[2,2,2]octylphenyl motif as HCV NS5A inhibitors. Compounds 2c, 4b and 6 have demonstrated low single-digit nM potency in gt-1a replicon and double-digit pM potency in gt-1b replicon, respectively. Moreover, both 4b and 6 have, respectively, exhibited good oral bioavailability in rats with a favorable liver/plasma ratio of the drug concentration.

Aliphatic Liquid Crystals, 9. - Stereospecific Reduction of 1-Acyl- to 1-Alkyl-4-phenylcyclohexanes

Sucrow, Wolfgang,Heider, RRoland,Joraschek, Norbert

, p. 1039 - 1044 (2007/10/02)

The title reaction - important for the synthesis of aliphatic liquid crystals - is accomplished by reduction of the tosylhydrazones with sodium cyanoborohydride.While the trans-configurated model ketones 6a, 7a give the tosylhydrazones 10a, 11a, and these

New phenylcyclohexyl- and cyclohexylphenylamines. Synthesis and pharmacological activity

De Meglio,Carissimi,Ravenna,Gentili

, p. 191 - 202 (2007/10/02)

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