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1,2-Cyclohexanediol, 3,5-bis(phenylmethoxy)-, (1R,2R,3R,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

671193-10-5

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671193-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 671193-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,1,1,9 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 671193-10:
(8*6)+(7*7)+(6*1)+(5*1)+(4*9)+(3*3)+(2*1)+(1*0)=155
155 % 10 = 5
So 671193-10-5 is a valid CAS Registry Number.

671193-10-5SDS

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 (1R,2R,3R,5R)-3,5-bis(phenylmethoxy)cyclohexane-1,2-diol

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:671193-10-5 SDS

671193-10-5Downstream Products

671193-10-5Relevant academic research and scientific papers

Synthesis and HIV-1 inhibitory activities of dicaffeoyl and digalloyl esters of quinic acid derivatives

Junior,Verde,Rezende,Caneschi,Couri,McDougall,Robinson Jr.,De Almeida

, p. 724 - 733 (2013/07/28)

Twenty analogues of the anti-HIV-1 integrase (IN) inhibitors dicaffeoylquinic acids (DCQAs) were prepared. Their IC50 values for 3'-end processing and strand transfer against recombinant HIV-1IN were determined in vitro, and their cell toxiciti

AKT INHIBITORS, PHARMACEUTICAL COMPOSITIONS, AND USES THEREOF

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Page 11-12, (2010/02/06)

Disclosed are inhibitors of the serine/threonine kinase Akt, pharmaceutical compositions comprising such inhibitors, and a method of preventing or treating a disease or condition in an animal by the use of such inhibitors. The Akt inhibitors have the form

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