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586415-12-5

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586415-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 586415-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,6,4,1 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 586415-12:
(8*5)+(7*8)+(6*6)+(5*4)+(4*1)+(3*5)+(2*1)+(1*2)=175
175 % 10 = 5
So 586415-12-5 is a valid CAS Registry Number.

586415-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(β,β-dichloroethenyl)-5-hydroxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2-(2,2-Dichlor-vinyl)-5-hydroxy-benzoesaeure

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:586415-12-5 SDS

586415-12-5Relevant articles and documents

Total synthesis and anti-viral activities of an extract of radix isatidis

He, Li-Wei,Chen, Yu-Qing,Yang, Jing-Yan,Wang, Tian-Lin,Li, Wei,Liu, Hua-Qing

, p. 20906 - 20912 (2014)

Radix isatidis (Banlangen), a famous traditional Chinese medicine, has been used for thousands of years in China due to its anti-viral activity. Through our research, we inferred that the anti-viral activity of Radix isatidis depended on the water-soluble

Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes

Hill, Ronald A.,Rudra, Sonali,Peng, Bo,Roane, David S.,Bounds, Jeffrey K.,Zhang, Yang,Adloo, Ahmad,Lu, Tiansheng

, p. 2099 - 2113 (2007/10/03)

We are seeking to discover potent CNS-active sulfonylureas with structural features that allow for the formation of several types of prodrugs. We report herein the syntheses of compounds comprising an initial series of hydroxyl-substituted analogues of the potent ATP-sensitive potassium channel blockers glyburide (glibenclamide) and gliquidone. Somewhat unexpectedly, several of the compounds were found to be comparably potent to glyburide as inhibitors of specific [3H]glyburide binding in rat brain preparations.

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