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39779-23-2

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39779-23-2 Usage

Synonyms

DMP

Type of compound

Organic compound

Structure

A derivative of pyrrole, which is a five-membered aromatic ring with one nitrogen atom

Functional groups

Two methoxy groups (-OCH3) attached to the phenyl ring

Usage

Research and drug development

Pharmacological properties

Analgesic, anti-inflammatory agent

Potential therapeutic applications

Treatment of neurological and psychiatric disorders

Ongoing research

Precise mechanisms of action and therapeutic applications are still under investigation

Check Digit Verification of cas no

The CAS Registry Mumber 39779-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,7 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39779-23:
(7*3)+(6*9)+(5*7)+(4*7)+(3*9)+(2*2)+(1*3)=172
172 % 10 = 2
So 39779-23-2 is a valid CAS Registry Number.

39779-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-dimethoxyphenyl)pyrrole

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:39779-23-2 SDS

39779-23-2Downstream Products

39779-23-2Relevant articles and documents

5-(N-Arylnortropan-3-yl)- and 5-(N-Arylpiperidin-4-yl)-2,4-diaminopyrimidines. Novel Inhibitors of Dihydrofolate Reductase

Maag, Hans,Locher, Rita,Daly, John J.,Kompis, Ivan

, p. 887 - 897 (2007/10/02)

Based on a computer-assisted analysis of the three-dimensional structure of the binary complex of E.coli dihydrofolate reductase (DHFR) with methotrexate, 5-(N-arylnortropan-3-yl)- and 5-(N-arylpiperidin-4-yl)-2,4-diaminopyrimidines 2 and 4 were designed

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