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118993-73-0

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118993-73-0 Usage

Chemical compound

4-[3-(bromomethyl)benzoyl]-2-Thiophenesulfonamide

Structure

Benzoyl-thiophene derivative with a sulfonamide group attached

Use

Building block for synthesis of drugs and bioactive molecules in the pharmaceutical industry

Reactivity

Versatile reagent for chemical reactions like nucleophilic substitution and palladium-catalyzed cross-coupling

Importance

Valuable compound in medicinal chemistry and drug discovery for its unique structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 118993-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,9 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118993-73:
(8*1)+(7*1)+(6*8)+(5*9)+(4*9)+(3*3)+(2*7)+(1*3)=170
170 % 10 = 0
So 118993-73-0 is a valid CAS Registry Number.

118993-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-Bromomethylbenzoyl)-thiophene-2-sulfonamide

1.2 Other means of identification

Product number -
Other names 4-(3-Bromomethyl-benzoyl)-thiophene-2-sulfonic acid amide

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:118993-73-0 SDS

118993-73-0Relevant articles and documents

4-Substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors

Hartman,Halczenko,Smith,Sugrue,Mallorga,Michelson,Randall,Schwam,Sondey

, p. 3822 - 3831 (2007/10/02)

A series of 4-substituted thiophene- and furan-2-sulfonamides was prepared and was found to possess nanomolar-level potency for inhibition of human carbonic anhydrase II in vitro. Selected examples from this group were further evaluated for their potentia

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