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4(1H)-Pyridinethione, 3-hydroxy-1,2-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209248-75-9

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209248-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209248-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,4 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 209248-75:
(8*2)+(7*0)+(6*9)+(5*2)+(4*4)+(3*8)+(2*7)+(1*5)=139
139 % 10 = 9
So 209248-75-9 is a valid CAS Registry Number.

209248-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-1,2-dimethylpyridine-4-thione

1.2 Other means of identification

Product number -
Other names 3-hydroxy-1,2-dimethyl-thiopyridone

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:209248-75-9 SDS

209248-75-9Relevant academic research and scientific papers

Chelator fragment libraries for targeting metalloproteinases

Agrawal, Arpita,Johnson, Sherida L.,Jacobsen, Jennifer A.,Miller, Melissa T.,Chen, Li-Hsing,Pellecchia, Maurizio,Cohen, Seth M.

, p. 195 - 199 (2010)

(Chemical Equation Presented) A chelator fragment library based on a variety of metal binding groups was screened against a metalloproteinase. Lead hits were identified and an expanded library of select compounds was synthesized, resulting in numerous high-affinity hits against several metalloprotein targets. The findings clearly demonstrate that chelators can be used to generate libraries suitable for fragment-based lead design (FBLD) directed at important metalloproteins.

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