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129993-24-4

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129993-24-4 Usage

Structure

A derivative of pyrrole, a five-membered aromatic heterocycle, with a 2-(2,5-dimethylphenyl) group and a 1-ethenyl group attached to the pyrrole ring.

Potential uses

Organic synthesis, drug discovery, and material science.

Unique value

The compound's unique structure and functional groups make it a valuable building block for the preparation of various advanced materials and pharmaceutical compounds.

Importance in research

Its properties and reactivity make it an important target for research and development in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 129993-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,9,9 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129993-24:
(8*1)+(7*2)+(6*9)+(5*9)+(4*9)+(3*3)+(2*2)+(1*4)=174
174 % 10 = 4
So 129993-24-4 is a valid CAS Registry Number.

129993-24-4SDS

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 2-(2,5-dimethylphenyl)-1-ethenylpyrrole

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:129993-24-4 SDS

129993-24-4Downstream Products

129993-24-4Relevant articles and documents

PYRROLES FROM KETOXIMES AND ACETYLENE. 46. PYRROLES WITH STERICALLY HINDERED SUBSTITUENTS

Aliev, I. A.,Korostova, S. E.,Mikhaleva, A. I.,Shevchenko, S. G.,Zeinalova, S. N.,et al.

, p. 1055 - 1058 (2007/10/02)

The corresponding pyrroles and their N-vinyl derivatives were obtained by the catalyzed (by an MOH-DMSO superbase) reaction of acetylene and its crypto forms (vinyl chloride, 1,2-dichloroethane) with alkyl-2,4-, alkyl-2,5-, and alkyl-3,4-dimethylphenylketoximes.Reaction intermediates - O-vinylketoximes - were detected.

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