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335030-18-7

335030-18-7

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335030-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335030-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,0,3 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 335030-18:
(8*3)+(7*3)+(6*5)+(5*0)+(4*3)+(3*0)+(2*1)+(1*8)=97
97 % 10 = 7
So 335030-18-7 is a valid CAS Registry Number.

335030-18-7SDS

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 benzyl 3-(6-aminopyridin-3-yl)acrylate

1.2 Other means of identification

Product number -
Other names benzyl (E)-3-(6-aminopyridin-3-yl)acrylate

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:335030-18-7 SDS

335030-18-7Relevant articles and documents

FAB I INHIBITORS

-

, (2008/06/13)

Compounds of the formula (I) are disclosed which are Fab I inhibitors and are useful in the treatment of bacterial infections.

Discovery of aminopyridine-based inhibitors of bacterial enoyl-ACP reductase (FabI)

Miller, William H.,Seefeld, Mark A.,Newlander, Kenneth A.,Uzinskas, Irene N.,Burgess, Walter J.,Heerding, Dirk A.,Yuan, Catherine C. K.,Head, Martha S.,Payne, David J.,Rittenhouse, Stephen F.,Moore, Terrance D.,Pearson, Stewart C.,Berry, Valerie,DeWolf Jr., Walter E.,Keller, Paul M.,Polizzi, Brian J.,Qiu, Xiayang,Janson, Cheryl A.,Huffman, William F.

, p. 3246 - 3256 (2007/10/03)

Bacterial enoyl-ACP reductase (FabI) catalyzes the final step in each cycle of bacterial fatty acid biosynthesis and is an attractive target for the development of new antibacterial agents. Our efforts to identify potent, selective FabI inhibitors began w

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