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40611-76-5

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40611-76-5 Usage

General Description

1H-Pyrrole-3-carboxylic acid, 5-Methyl-, Methyl ester is a chemical compound that is composed of a pyrrole ring with a carboxylic acid group at position 3 and a methyl ester group at position 5. It is commonly used in the production of pharmaceuticals and fine chemicals. 1H-Pyrrole-3-carboxylic acid, 5-Methyl-, Methyl ester has been found to have various biological activities, including anti-inflammatory and anti-cancer properties. It is also used in the synthesis of various organic compounds and is a versatile building block in organic chemistry. Additionally, it has potential applications in the development of new drugs and medical treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 40611-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,1 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40611-76:
(7*4)+(6*0)+(5*6)+(4*1)+(3*1)+(2*7)+(1*6)=85
85 % 10 = 5
So 40611-76-5 is a valid CAS Registry Number.

40611-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-methyl-1H-pyrrole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Pyridinecarboxylic acid,5-methyl-,methyl ester,1-oxide

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:40611-76-5 SDS

40611-76-5Relevant articles and documents

PHTHALAZINONE DERIVATIVES

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Page/Page column 43-44, (2009/08/14)

A compound of the formula (I): wherein: A and B together represent an optionally substituted, fused aromatic ring; X and Y are selected from CH and CH, CF and CH, CH and CF and N and CH respectively; RC is selected from H, C1-4 alkyl

Carbene and Silicon Routes toward a Simple Nitrile Ylide. Spectroscopic, Kinetic, and Chemical Characterization

Turro, Nicholas J.,Cha, Yuan,Gould, Ian R.,Padwa, Albert,Gasdaska, John R.,Tomas, Miguel

, p. 4415 - 4417 (2007/10/02)

The generation and characterization of methyl nitrile ylide photochemically by addition of singlet methylene to acetonitrile and chemically from silylthioimidate and subsequent dipolar cycloaddition are carried out.

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