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methyl 1-(4-nitrophenyl)-1H-pyrrole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124475-67-8

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124475-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124475-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,7 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124475-67:
(8*1)+(7*2)+(6*4)+(5*4)+(4*7)+(3*5)+(2*6)+(1*7)=128
128 % 10 = 8
So 124475-67-8 is a valid CAS Registry Number.

124475-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-nitrophenyl)-pyrrole-2-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl 1-(4-nitrophenyl)pyrrole-2-carboxylate

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:124475-67-8 SDS

124475-67-8Relevant academic research and scientific papers

HETEROCYCLIC UREA COMPOUNDS

-

Page/Page column 61, (2013/07/05)

The present invention provides a compound of the following formula, racemates, enantiomers and salts thereof. Also provided is the use of these compounds as antibacterials, compositions comprising them and processes for their manufacture

Palladium-catalyzed decarboxylative cross-coupling reaction between heteroaromatic Carboxylic acids and Aryl halides

Bilodeau, Francois,Brochu, Marie-Christine,Guimond, Nicolas,Thesen, Kris H.,Forgione, Pat

experimental part, p. 1550 - 1560 (2010/06/12)

"Chemical Equation Presented" A full overview of the decarboxylative cross-coupling reaction between heteroaromatic carboxylic acids and aryl halides is described. This transformation employs palladium catalysts with short reaction times providing facile synthesis of aryl-substituted heteroaromatics. The effect of each reaction parameter including solvent, base, and additive employed as well as the full substrate scope of this transformation are reported. Mechanistic evidence is also disclosed that sheds light on possible reaction pathways.

SPATIAL STRUCTURE OF DERIVATIVES OF 1-NITROPHENYLPYRROLES

Pina, M. del' K.,Budylin, V. A.,Rodriges, M.,Bundel', Yu. G.

, p. 146 - 151 (2007/10/02)

Combined 1H and 13C NMR data were used to show that 2-carbonyl derivatives of 1-nitrophenylpyrroles (aldehydes, acids, esters, and amides) have primarily the s-trans-configuration.Oximes of 1-nitrophenyl-2-formylpyrroles exist as a mixture of s-trans-syn-

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