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129706-46-3

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129706-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129706-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,0 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129706-46:
(8*1)+(7*2)+(6*9)+(5*7)+(4*0)+(3*6)+(2*4)+(1*6)=143
143 % 10 = 3
So 129706-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H19NO3S2/c17-14(4-2-1-3-13-9-10-20-21-13)16-12-7-5-11(6-8-12)15(18)19/h5-8,13H,1-4,9-10H2,(H,16,17)(H,18,19)/t13-/m1/s1

129706-46-3SDS

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 4-({5-[(3R)-1,2-Dithiolan-3-yl]pentanoyl}amino)benzoic acid

1.2 Other means of identification

Product number -
Other names N-Pentafluorophenylmethylene-benzene-1,2-diamine

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:129706-46-3 SDS

129706-46-3Downstream Products

129706-46-3Relevant articles and documents

Lipoic acid analogs with enhanced pharmacological activity

Kates, Steven A.,Casale, Ralph A.,Baguisi, Alexander,Beeuwkes III, Reinier

, p. 505 - 512 (2014)

Lipoic acid (1,2-dithiolane-3-pentanoic acid) is a pharmacophore with unique antioxidant and cytoprotective properties. We synthesized a library based upon the condensation of natural and unnatural amino acids with the carboxylic acid moiety of lipoic acid. SAR studies were conducted using a cardiac ischemia-reperfusion animal model. Cytoprotective efficacy was associated with the R-enantiomer of the dithiolane. Potency of library compounds was dictated by the acidic strength of the adduct. α-N-[(R)-1,2-dithiolane-3-pentanoyl]- l-glutamyl-l-alanine, designated CMX-2043, was chosen for further pharmacologic evaluation.

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