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50691-37-7

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50691-37-7 Usage

Structure

Five-membered aromatic ring with one nitrogen atom and two methyl groups attached to the second and fourth positions, and a phenyl group attached to the first position.

Type of compound

Substituted pyrrole derivative

Usage

Organic chemistry and pharmaceutical research

Potential applications

Building block in the synthesis of various pharmaceuticals and agrochemicals

Biological activities

Potential antibacterial and antifungal properties

Importance

Valuable target for drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 50691-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,9 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50691-37:
(7*5)+(6*0)+(5*6)+(4*9)+(3*1)+(2*3)+(1*7)=117
117 % 10 = 7
So 50691-37-7 is a valid CAS Registry Number.

50691-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethyl-1-phenylpyrrole

1.2 Other means of identification

Product number -
Other names 2,4-dimethyl-1-phenyl-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:50691-37-7 SDS

50691-37-7Downstream Products

50691-37-7Relevant articles and documents

Synthesis of 1,2,3,5-tetrasubstituted pyrrole derivatives from 2-(2-bromoallyl)-1,3-dicarbonyl compounds

Demir, Ayhan S,Akhmedov, Idris M,Sesenoglu, ?zge

, p. 9793 - 9799 (2007/10/03)

2-(2-Bromoallyl)-1,3-dicarbonyl compounds are converted into β-enamino, β-hydrazino esters and ketones, followed by base-promoted cyclization, leading to the formation of the corresponding 1,2,3,5-tetrasubstituted pyrroles. 1,2,4- and 1,2,3,4-Substituted pyrroles are also isolated as minor products. Starting from the 2-(2-bromoallyl)-cyclohexane-1,3-dione the corresponding tetrahydro indolone is prepared in good yield.

A photochemical preparation of N substituted pyrroles from pyridazine N oxides

Tsuchiya,Arai,Igeta

, p. 1516 - 1519 (2007/10/04)

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