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6341-35-1

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6341-35-1 Usage

General Description

4-Fluoro-N-(furan-2-ylmethyl)benzenesulfonamide is a specialized chemical compound known for its distinctive structure and properties. Featuring a fluoro-substituted benzene ring linked to a sulfonamide group, as well as marked by the presence of a furan ring, this compound is characterized by heteroaromaticity and electron-rich attributes. Although specific applications and reactions can vary, its synthesis and use primarily reside in advanced chemical research, including in the development of pharmaceuticals where sulfonamide derivatives often exhibit antimicrobial properties. Its unique molecular structure also makes it suitable for various chemical transformations, including coupling reactions. Overall, this compound represents a key chemical entity in the realm of organic and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 6341-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6341-35:
(6*6)+(5*3)+(4*4)+(3*1)+(2*3)+(1*5)=81
81 % 10 = 1
So 6341-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H10FNO3S/c12-9-3-5-11(6-4-9)17(14,15)13-8-10-2-1-7-16-10/h1-7,13H,8H2

6341-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-N-(furan-2-ylmethyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-(FURAN-2-YLMETHYL) 4-FLUOROBENZENESULFONAMIDE

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:6341-35-1 SDS

6341-35-1Downstream Products

6341-35-1Relevant articles and documents

Formal substitution of bromocyclopropanes with nitrogen nucleophiles

Banning, Joseph E.,Gentillon, Jacob,Ryabchuk, Pavel G.,Prosser, Anthony R.,Rogers, Andrew,Edwards, Andrew,Holtzen, Andrew,Babkov, Ivan A.,Rubina, Marina,Rubin, Michael

, p. 7601 - 7616 (2013)

A highly chemo- and diastereoselective protocol toward amino-substituted donor-acceptor cyclopropanes via the formal nucleophilic displacement in bromocyclopropanes is described. A wide range of N-nucleophiles, including carboxamides, sulfonamides, azoles, and anilines, can be efficiently employed in this transformation, providing expeditious access to stereochemically defined and densely functionalized cyclopropylamine derivatives.

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