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4-(2-NITRO-PHENYL)-3-OXO-BUTYRIC ACID METHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119209-56-2

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119209-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119209-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,2,0 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 119209-56:
(8*1)+(7*1)+(6*9)+(5*2)+(4*0)+(3*9)+(2*5)+(1*6)=122
122 % 10 = 2
So 119209-56-2 is a valid CAS Registry Number.

119209-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-NITRO-PHENYL)-3-OXO-BUTYRIC ACID METHYL ESTER

1.2 Other means of identification

Product number -
Other names -

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:119209-56-2 SDS

119209-56-2Relevant academic research and scientific papers

Expedient synthesis of 3-hydroxyisoquinolines and 2-hydroxy-1,4- naphthoquinones via one-pot aryne acyl-alkylation/condensation

Allan, Kevin M.,Hong, Boram D.,Stoltz, Brian M.

supporting information; experimental part, p. 4960 - 4964 (2010/02/15)

A convenient method is disclosed for the synthesis of both 3-hydroxyisoquinolines and 2-hydroxy-1,4-naphthoquinones from β-ketoesters using a one-pot aryne acyl-alkylation/condensation procedure. When performed in conjunction with a one-step method for the synthesis of the β-ketoester substrates, this method provides a new route to these polyaromatic structures in only two steps from commercially available carboxylic acid starting materials. The utility of this approach is demonstrated in the synthesis of the atropisomeric P,N-ligand, QUINAP. The Royal Society of Chemistry 2009.

Synthesis of pyrazole derivatives 4(1H)-quinolone and 4-chloroquinoline by thermolysis of arylaminomethylene Meldrum's acid derivative

Peng, Lizeng,Zhang, Tao,Li, Ying,Li, Yulin

, p. 785 - 791 (2007/10/03)

Efficient syntheses of 4(1H)-quinolone 1 and 4-chloroquinoline 2 by thermolysis of arylaminomethylene Meldrum's acid derivative starting from 2-nitrophenyl acetic acid.

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