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32928-30-6

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32928-30-6 Usage

Structure

Substituted pyrrole derivative with a carboxaldehyde group

Usage

Organic synthesis, pharmaceutical research

Potential applications

Building block for synthesis of complex molecules, starting material for production of pharmaceutical drugs or other biologically active compounds

Versatility

Various interesting properties and potential applications due to its unique molecular structure

Value

A potentially valuable compound for use in various fields of science and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 32928-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,2 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32928-30:
(7*3)+(6*2)+(5*9)+(4*2)+(3*8)+(2*3)+(1*0)=116
116 % 10 = 6
So 32928-30-6 is a valid CAS Registry Number.

32928-30-6SDS

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 3-ethyl-4-methyl-1H-pyrrole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-ethyl-4-methyl-pyrrole-2-carbaldehyde

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:32928-30-6 SDS

32928-30-6Relevant articles and documents

Regiocontrolled synthesis of pyrrole-2-carboxaldehydes and 3-pyrrolin-2-ones from pyrrole Weinreb amides

Coffin, Aaron R.,Roussell, Michael A.,Tserlin, Elina,Pelkey, Erin T.

, p. 6678 - 6681 (2007/10/03)

A regiocontrolled synthesis of 3,4-disubstituted pyrrole-2-carboxaldehydes was completed in two steps from acyclic starting materials. A Barton-Zard pyrrole synthesis between N-methoxy-N-methyl-2-isocyanoacetamide and α-nitroalkenes or β-nitroacetates provided N-methoxy-N-methyl pyrrole-2-carboxamides (pyrrole Weinreb amides), which were converted into the corresponding pyrrole-2-carboxaldehydes by treatment with lithium aluminum hydride. A regioselective oxidation of the pyrrole-2-carboxaldehydes gave the corresponding 3,4-disubstituted 3-pyrrolin-2-ones.

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