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Ethanone, 2-chloro-1-(1-ethyl-1H-pyrrol-3-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126624-56-4

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126624-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126624-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,6,2 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 126624-56:
(8*1)+(7*2)+(6*6)+(5*6)+(4*2)+(3*4)+(2*5)+(1*6)=124
124 % 10 = 4
So 126624-56-4 is a valid CAS Registry Number.

126624-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Ethyl-3-chloroacetylpyrrole

1.2 Other means of identification

Product number -
Other names 2-Chloro-1-(1-ethyl-1H-pyrrol-3-yl)-ethanone

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:126624-56-4 SDS

126624-56-4Downstream Products

126624-56-4Relevant academic research and scientific papers

Selective α-Chlorination of Acetylpyrroles

Croce, Piero Dalla,Ferraccioli, Rafaella,Ritieni, Alberto

, p. 212 - 213 (2007/10/02)

Reaction of acetylpyrroles with benzyltrimethylammonium dichloroiodate in tetrahydrofuran solution leads to the corresponding α-chloro derivatives with high selectivity and good yields.

Direct Vilsmeier-Haack Chloroacetylation of Pyrroles

Croce, Piero Dalla,Rosa, Concetta La,Ritieni, Alberto

, p. 783 - 784 (2007/10/02)

Reaction of pyrroles with N,N-dimethyl-2-chloroacetamide in the presence of phosphorus oxychloride leads to a mixture of 2- and 3-chloroacetylpyrroles, which can be separated by chromatography.

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