871269-13-5

Basic information

• Product Name: 4-(3-BROMOPHENYLSULFONYL)MORPHOLINE
• Synonyms: 4-(3-BROMOPHENYLSULFONYL)MORPHOLINE;4-[(3-BROMOPHENYL)SULPHONYL]MORPHOLINE;4-[(3-Bromophenyl)sulphonyl]morpholine 95%;4-[(3-Bromobenzene)sulfonyl]morpholine;4-[(3-Bromophenyl)sulphonyl]morpholine95%
• CAS NO: 871269-13-5
• Molecular Formula: C₁₀H₁₂BrNO₃S
• Molecular Weight: 306.18
• Product Categories: blocks;Bromides;Heterocycles;Sulfonamides;alkyl bromide
• Mol File: 871269-13-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 132-136
• Boiling Point: 427.2 °C at 760 mmHg
• Flash Point: 212.2 °C
• Appearance: /
• Density: 1.594g/cm³
• Vapor Pressure: 1.67E-07mmHg at 25°C
• Refractive Index: 1.596
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(3-BROMOPHENYLSULFONYL)MORPHOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-BROMOPHENYLSULFONYL)MORPHOLINE(871269-13-5)
• EPA Substance Registry System: 4-(3-BROMOPHENYLSULFONYL)MORPHOLINE(871269-13-5)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 871269-13-5(Hazardous Substances Data)

Usage

General Description

4-(3-bromophenylsulfonyl)morpholine is a chemical compound with the molecular formula C11H12BrNO3S. It is a morpholine derivative with a sulfonyl group attached to a bromophenyl ring. 4-(3-BROMOPHENYLSULFONYL)MORPHOLINE is commonly used as a reagent in organic synthesis and pharmaceutical research. Its properties make it a useful building block for the synthesis of various biologically active compounds. It is also known for its potential as an antimicrobial agent and has been studied for its potential applications in medicine. Additionally, it has been utilized in the development of new materials and chemical processes.

InChI:InChI=1/C10H12BrNO3S/c11-9-2-1-3-10(8-9)16(13,14)12-4-6-15-7-5-12/h1-3,8H,4-7H2

Upstream product

• 110-91-8 morpholine 
• 2905-24-0 3-Bromobenzenesulfonyl chloride 
• 89598-96-9 (3-bromophenyl)boronic acid 
• 591-18-4 1-Bromo-3-iodobenzene 

Downstream Products

• 1020736-13-3 8-chloro-3-methyl-4-{3-[3-(morpholin-4-ylsulfonyl)phenoxy]phenyl}quinoline 
• 1225279-68-4 4-[3-(quinoxalin-6-yl)phenylsulfonyl]morpholine 

Relevant articles and documents

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The formation of carbon-carbon bonds lies at the heart of synthetic organic chemistry and is widely applied to construct complex drugs, polymers, and materials. Despite its importance, catalytic carbonyl arylation remains comparatively underdeveloped, due

One-Pot Sulfonamide Synthesis Exploiting the Palladium-Catalyzed Sulfination of Aryl Iodides

Aryl ammonium sulfinates, conveniently prepared from aryl iodides and the sulfur dioxide surrogate DABSO, under the action of a palladium(0) catalyst, are transformed in a one-pot process to a variety of functionalized sulfonamides. The sulfinate to sulfonamide transformation is achieved by simple treatment with an aqueous solution of the relevant amine and sodium hypochlorite (bleach). A broad range of amines, including anilines, and amino acid derivatives, are combined efficiently with a variety of aryl iodides, leading to sulfonamides in high yields.

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