116547-91-2

Basic information

• Product Name: N-(2-Bromophenyl)methansulfonamide
• Synonyms: N-(2-Bromophenyl)methansulfonamide;Methanesulfonamide, N-(2-bromophenyl)-
• CAS NO: 116547-91-2
• Molecular Formula: C₇H₈BrNO₂S
• Molecular Weight: 250.11
• Product Categories: Aryl;Organohalides
• Mol File: 116547-91-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-Bromophenyl)methansulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Bromophenyl)methansulfonamide(116547-91-2)
• EPA Substance Registry System: N-(2-Bromophenyl)methansulfonamide(116547-91-2)

Safety Data

• Hazardous Substances Data: 116547-91-2(Hazardous Substances Data)

Usage

General Description

N-(2-Bromophenyl)methansulfonamide is a chemical compound with the molecular formula C7H7BrNO2S. It is an organosulfonamide derivative and belongs to the class of sulfonamides, which are compounds commonly used as antibiotics and antifungal agents. This particular compound is a white powder that is insoluble in water but soluble in organic solvents. It is used in the synthesis of pharmaceuticals and agrochemicals, and it has potential applications in the field of medicinal chemistry as a building block for developing new drugs. The bromine atom attached to the phenyl ring gives the compound unique chemical properties and makes it useful for various scientific and industrial applications.

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 615-36-1 2-bromoaniline 

Downstream Products

• 7022-25-5 N-(2-methoxyphenyl)methanesulfonamide 
• 1206901-63-4 N-(but-2-enyl)-N-(2-bromophenyl)-methanesulfonamide 
• 1206901-65-6 N-(2-bromophenyl)-N-(cyclohex-2-enyl)methanesulfonamide 
• 1206901-64-5 N-(2-bromophenyl)-N-(3-methylbut-2-enyl)methanesulfonamide 
• 553652-34-9 N-(2-bromophenyl)-N-methylmethanesulfonamide 
• 1257705-85-3 N-methyl-N-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-methane-sulfonamide 
• 229-87-8 phenanthridine 
• 1197-22-4 N-phenylmethanesulfonamide 

Relevant articles and documents

Synthesis of spiropyrrolidinyl-benzoisothiazoline derivatives by 1,3-dipolar cycloaddition of benzoisothiazole-2,2-dioxide-3-ylidenes and azomethine ylide

The new spirocyclic compounds, spiropyrrolidinyl-benzoisothiazoline derivatives were synthesized by the 1,3-dipolar cycloaddition of benzoisothiazole-2,2-dioxide-3-ylidenes and azomethine ylide. The stereochemistry of 1,3-dipolar cycloaddition as well as the stereochemistry of Knoevenagel condensation of benzoisothiazole-2,2-dioxide with aldehydes were studied.

FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF

Disclosed area fused ring pyrimidine compound, and an intermediate, a preparation method, a composition and a use thereof. The fused ring pyrimidine compound is a compound as shown in formula I, a tautomer, an enantiomer, a diastereoisomer, a pharmaceutically acceptable salt, a metabolite, a metabolic precursor or a prodrug thereof, wherein the above-mentioned compound is used for the preparation of a medicine for preventing, remitting or treating one or more of immune system diseases, autoimmune diseases, cell proliferative diseases, allergic disorders and cardiovascular diseases, and the compound has a strong inhibitory effect on the Janues kinase, FGFR kinase, FLT3 kinase and Src family kinase.

Self-induced stereoselective in situ trifluoromethylation: Preparation of spiro[indoline-3,3′-quinoline] via palladium-catalyzed cascade reaction

An efficient method to prepare 1′H-spiro[indoline-3,3′- quinoline]-2′,4′-diones and their trifluoromethylated products was developed via a palladium-catalyzed Sonogashira coupling/Wacker-type oxypalladation/cyclization cascade reaction. The amount of wate