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1H-Pyrrole-3,4-dicarboxaldehyde, 1-methyl- is an organic compound with the chemical formula C7H7NO2. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom. The molecule features two formyl groups (aldehyde groups) attached to the third and fourth carbon atoms of the pyrrole ring, and a methyl group attached to the first carbon atom. 1H-Pyrrole-3,4-dicarboxaldehyde, 1-methyl- is known for its potential applications in the synthesis of various heterocyclic compounds and pharmaceuticals, as well as its use as a building block in organic chemistry. Due to its reactivity and unique structure, it is an important intermediate in the preparation of various biologically active molecules and materials.

51110-65-7

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51110-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51110-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,1 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51110-65:
(7*5)+(6*1)+(5*1)+(4*1)+(3*0)+(2*6)+(1*5)=67
67 % 10 = 7
So 51110-65-7 is a valid CAS Registry Number.

51110-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylpyrrole-3,4-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names methyl-1 diformyl-3,4 1H-pyrrole

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:51110-65-7 SDS

51110-65-7Relevant academic research and scientific papers

PYRROLE CHEMISTRY. XXIV. THE VILSMEIER FORMYLATION AND CYANATION OF PYRROLE ACETALS. A SYNTHESIS OF PYRROLE-2,3,5-TRICARBOXALDEHYDE

Loader, Charles E.,Barnett, Graham H.,Anderson, Hugh J.

, p. 383 - 389 (2007/10/02)

The preparation of the acetals of a number of pyrrole mono- and dicarboxaldehydes is described.It is shown that, provided the reactivity of the unsubstituted ring positions on the pyrrole nucleus is not too low, a carboxaldehyde or a carbonitrile group may be substituted on the pyrrole ring using the Vilsmeier reaction or chlorosulfonyl isocyanate respectively. Vilsmeier formylation of the diacetal, 2,4-di(5,5-dimethyl-1,3-dioxan-2-yl)-pyrrole, followed by hydrolysis gave pyrrole-2,3,5-tricarboxaldehyde.

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