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2-Propenoic acid, 3-[8-[[[4-(1,1-dimethylethyl)-2-thiazolyl]amino]carbonyl]-4-oxo-2-phenyl-4 H-pyrido[1,2-a]pyrimidin-3-yl]-, 1,1-dimethylethyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

881997-19-9

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881997-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881997-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,9,9 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 881997-19:
(8*8)+(7*8)+(6*1)+(5*9)+(4*9)+(3*7)+(2*1)+(1*9)=239
239 % 10 = 9
So 881997-19-9 is a valid CAS Registry Number.

881997-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (2E)-3-(8-{[(4-tert-butyl-1,3-thiazol-2-yl)amino]carbonyl}-4-oxo-2-phenyl-4H-pyrido[1,2-a]pyrimidin-3-yl)acrylate

1.2 Other means of identification

Product number -
Other names (E)-3-[8-(4-tert-Butyl-thiazol-2-ylcarbamoyl)-4-oxo-2-phenyl-4H-pyrido[1,2-a]pyrimidin-3-yl]-acrylic acid tert-butyl ester

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:881997-19-9 SDS

881997-19-9Downstream Products

881997-19-9Relevant academic research and scientific papers

MexAB-OprM specific efflux pump inhibitors in Pseudomonas aeruginosa. Part 5: Carbon-substituted analogues at the C-2 position

Yoshida, Ken-Ichi,Nakayama, Kiyoshi,Kuru, Noriko,Kobayashi, Shozo,Ohtsuka, Masami,Takemura, Makoto,Hoshino, Kazuki,Kanda, Hiroko,Zhang, Jason Z.,Lee, Ving J.,Watkins, William J.

, p. 1993 - 2004 (2007/10/03)

A series of 4-oxo-4H-pyrido[1,2-a]pyrimidine derivatives, derivatized at the 2-position with carbon-linked substituents, were synthesized and evaluated for their ability to potentiate the activity of the fluoroquinolone levofloxacin (LVFX) and the anti-pseudomonas β-lactam aztreonam (AZT) in Pseudomonas aeruginosa. Palladium-catalyzed cross-coupling methods were applied for the incorporation of aliphatic and aromatic substituents.

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