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19247-73-5

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19247-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19247-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,4 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19247-73:
(7*1)+(6*9)+(5*2)+(4*4)+(3*7)+(2*7)+(1*3)=125
125 % 10 = 5
So 19247-73-5 is a valid CAS Registry Number.

19247-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopentanesulfonic acid

1.2 Other means of identification

Product number -
Other names CyclopentansulfonsAfA currencyure

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:19247-73-5 SDS

19247-73-5Relevant academic research and scientific papers

Design of potent and selective 2-aminobenzimidazole-based p38α MAP kinase inhibitors with excellent in vivo efficacy

De Dios, Alfonso,Shih, Chuan,López De Uralde, Beatriz,Sánchez, Concepción,Del Prado, Miriam,Martín Cabrejas, Luisa M.,Pleite, Sehila,Blanco-Urgoiti, Jaime,Lorite, María José,Nevill Jr., C. Richard,Bonjouklian, Rosanne,York, Jeremy,Vieth, Michal,Wang, Yong,Magnus, Nicholas,Campbell, Robert M.,Anderson, Bryan D.,McCann, Denis J.,Giera, Deborah D.,Lee, Paul A.,Schultz, Richard M.,Li, Li C.,Johnson, Lea M.,Wolos, Jeffrey A.

, p. 2270 - 2273 (2007/10/03)

We report the design and discovery of a 2-amino-benzimidazole-based series of potent and highly selective p38α inhibitors. The lead compound 1 had low-nanomolar activity in both ATP competitive enzyme binding and inhibition of TNFα release in macrophages.

Mercury-Photosensitized Sulfination, Hydrosulfination, and Carbonylation of Hydrocarbons: Alkane and Alkene Conversion to Sulfonic Acids, Ketones, and Aldehydes

Ferguson, Richard R.,Crabtree, Robert H.

, p. 5503 - 5510 (2007/10/02)

Mercury-photosensitized sulfination of alkanes, RH, with SO2 forms sulfinic acids (RSOOH) and sulfinate esters (RSOOR) in high conversion and yield; oxidation of the mixture produces RSO2OH in high yield.Mercury-photosensitized hydrosulfination of alkenes with H2 and SO2 gives RSO2OH after oxidative workup.Mercury-photosensitized carbonylation of alkanes with CO gives RCHO and R2CO.

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