63132-74-1

Basic information

• Product Name: N-(2-bromoethyl)methanesulfonamide
• Synonyms: N-(2-bromoethyl)methanesulfonamide;MethanesulfonaMide,N-(2-broMoethyl)-
• CAS NO: 63132-74-1
• Molecular Formula: C₃H₈BrNO₂S
• Molecular Weight: 202.07
• Mol File: 63132-74-1.mol
• Article Data: 9

Chemical Properties

• Melting Point: 47-49 °C
• Boiling Point: 263.1°C at 760 mmHg
• Flash Point: 112.9°C
• Appearance: /
• Density: 1.668g/cm³
• Vapor Pressure: 0.0105mmHg at 25°C
• Refractive Index: 1.508
• PKA: 9.83±0.40(Predicted)
• CAS DataBase Reference: N-(2-bromoethyl)methanesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-bromoethyl)methanesulfonamide(63132-74-1)
• EPA Substance Registry System: N-(2-bromoethyl)methanesulfonamide(63132-74-1)

Safety Data

• Hazardous Substances Data: 63132-74-1(Hazardous Substances Data)

Usage

General Description

N-(2-bromoethyl)methanesulfonamide is a chemical compound that belongs to the class of sulfonamides, which are organic compounds containing a sulfonamide functional group. It is a sulfonamide derivative with a bromoethyl substituent attached to the nitrogen atom. Sulfonamides are known for their antimicrobial properties and have been widely used as antibacterial and antifungal agents. The bromoethyl group in N-(2-bromoethyl)methanesulfonamide makes it potentially useful for chemical synthesis, as it can be used as a reactive intermediate in organic reactions. N-(2-bromoethyl)methanesulfonamide may also have potential applications in pharmaceutical research for the development of new drugs.

InChI:InChI=1/C3H8BrNO2S/c1-8(6,7)5-3-2-4/h5H,2-3H2,1H3

Upstream product

• 107-09-5 2-bromoethylamine 
• 124-63-0 methanesulfonyl chloride 
• 2576-47-8 2-bromoethylamine hydrobromide 

Downstream Products

• 1450604-06-4 C₁₉H₂₆N₂O₆S₂ 
• 71045-92-6 N-[2-(4-hydroxy-N-methyl-anilino)-ethyl]-methanesulfonamide 

Relevant articles and documents

Synthesis of C- and N-Substituted 1,5,2,6-Dithiadiazocanes –Electrophilic-Nucleophilic Thioamination (ENTA) Reagents

A synthetic method is presented for S?N bond formation starting from cheap and affordable materials. We show that (un)substituted N-protected cyclic eight-membered C2-symmetric sulfenamides have been prepared in a few steps using this procedure. The synthetic utility of these ambipolar derivatives was demonstrated in a variety of synthetic transformations affording different S,N-heterocyles of pharmaceutical relevance in one or two steps from simple starting materials. (Figure presented.).

NOVEL DIHYDROQUINOLIZINONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

The invention provides novel compounds having the general formula (I) wherein R1, R2 R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds in the treatment of the hepatitis B virus.

NOVEL OXABISPIDINE COMPOUNDS AND THEIR USE IN THE TREATMENT OF CARDIAC ARRHYTHMIAS

There is provided compounds of formula I, wherein R1, R2, R4, R41 to R46, A, B and G have meanings given in the description, which are useful in the prophylaxis and in the treatment of arrhythmias, in particular atrial and ventricular arrhythmias.