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1H-Pyrrole, 3-ethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63045-63-6

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63045-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63045-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63045-63:
(7*6)+(6*3)+(5*0)+(4*4)+(3*5)+(2*6)+(1*3)=106
106 % 10 = 6
So 63045-63-6 is a valid CAS Registry Number.

63045-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-2-phenyl-1H-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:63045-63-6 SDS

63045-63-6Relevant academic research and scientific papers

C-vinylation of 1-vinylpyrroles with benzoylacetylene on silica gel

Trofimov,Stepanova,Sobenina,Mikhaleva,Ushakov,Elokhina

, p. 1878 - 1882 (2007/10/03)

1-Vinylpyrroles readily add to benzoylacetylene on grinding the reagents with silica gel at room temperature to form 2-(E)-(2-benzoylvinyl)-1-vinylpyrroles in 50-84% yield in a regioand stereoselective manner.

PYRROLES FROM KETOXIMES AND ACETYLENE. 30. THE SYNTHESIS OF 3-ALKYL-2-ARYLPYRROLES

Korostova, S. E.,Mikhaleva, A. I.,Sobenina, L. N.,Shevchenko, S. G.,Shcherbakov, V. V.

, p. 1238 - 1241 (2007/10/02)

Conditions were found for the synthesis of 3-alkyl-2-arylpyrroles using the Trofimov reaction at 50-70 deg C both at elevated and atmospheric pressure.O-Vinyloximes and 3H-5-hydroxy-4,5-dihydropyrroles were isolated as intermediates.

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