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951883-97-9

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951883-97-9 Usage

General Description

1-(5-Bromo-1H-pyrrol-2-yl)-2,2,2-trichloroethanone is a chemical compound with the formula C6H3BrCl3NO. It is a trichloroethanone derivative with a bromine-substituted pyrrole group. 1-(5-Bromo-1H-pyrrol-2-yl)-2,2,2-trichloroethanone is commonly used as a reagent in organic chemistry and is known for its ability to undergo various chemical reactions. It is also used in the synthesis of pharmaceuticals and agrochemicals due to its unique chemical properties. Additionally, it is considered to be a valuable building block for the production of organic compounds, making it an important tool in chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 951883-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,8,8 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 951883-97:
(8*9)+(7*5)+(6*1)+(5*8)+(4*8)+(3*3)+(2*9)+(1*7)=219
219 % 10 = 9
So 951883-97-9 is a valid CAS Registry Number.

951883-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-Bromo-1H-pyrrol-2-yl)-2,2,2-trichloroethanone

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

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More Details:951883-97-9 SDS

951883-97-9Downstream Products

951883-97-9Relevant articles and documents

Substrate Controlled Regioselective Bromination of Acylated Pyrroles Using Tetrabutylammonium Tribromide (TBABr3)

Gao, Shuang,Bethel, Travis K.,Kakeshpour, Tayeb,Hubbell, Grace E.,Jackson, James E.,Tepe, Jetze J.

, p. 9250 - 9255 (2018/07/15)

Electrophilic bromination of pyrroles bearing carbonyl substituents at C-2 typically results in a mixture of the 4- and 5-brominated species, generally favoring the 4-position. Herein, we describe a substrate-controlled regioselective bromination in which

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