951883-92-4

Basic information

• Product Name: N-Propyl 2-bromobenzenesulfonamide
• Synonyms: 2-Bromo-N-propylbenzenesulfonamide;N-Propyl 2-bromobenzenesulfonamide
• CAS NO: 951883-92-4
• Molecular Formula: C₉H₁₂BrNO₂S
• Molecular Weight: 278.17
• Product Categories: blocks;Bromides;Sulfonamides
• Mol File: 951883-92-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N-Propyl 2-bromobenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Propyl 2-bromobenzenesulfonamide(951883-92-4)
• EPA Substance Registry System: N-Propyl 2-bromobenzenesulfonamide(951883-92-4)

Safety Data

• Hazardous Substances Data: 951883-92-4(Hazardous Substances Data)

Usage

General Description

N-Propyl 2-bromobenzenesulfonamide is a chemical compound with the molecular formula C9H12BrNO2S. It is a sulfonamide derivative with a propyl group attached to the nitrogen atom and a bromine atom attached to the benzene ring. N-Propyl 2-bromobenzenesulfonamide has various applications in the pharmaceutical and chemical industries, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It can also be used as a reagent in organic synthesis and as a building block in the production of various organic compounds. N-Propyl 2-bromobenzenesulfonamide may also have biological activity and could potentially be used in biological research and drug development.

Upstream product

• 107-10-8 propylamine 
• 2905-25-1 o-bromobenzenesulfonyl chloride 
• 7154-66-7 2-bromobenzoic acid chloride 

Relevant articles and documents

Diastereoselective synthesis of 1,3-disubstituted isoindolines and sultams via bronsted acid catalysis

The bis(trifluoromethane)sulfonimide (Tf2NH) catalyzed intramolecular hydroamidation of terminal alkynes is reported. The combination of Et3SiH and Tf2NH provides cis-1,3-disubstituted isoindolines and sultams in high yield (up to 98%) and high diastereoselectivity (up to 99?:?1 d.r.).

Palladium-catalyzed C-C coupling of aryl halides with isocyanides: An alternative method for the stereoselective synthesis of (3E)-(Imino)isoindolin- 1-ones and (3E)-(imino)thiaisoindoline 1,1-dioxides

A palladium-catalyzed, one-pot cyclization reaction to construct (3E)-(imino)isoindolin-1-ones and (3E)-(imino)thiaisoindoline 1,1-dioxides by introducing ortho-reactive functional groups on aryl halides is reported. Under optimal conditions, the cyclization reaction afforded the corresponding products in good to excellent yields (up to 93%) with high stereoselectivity. Notably, this transformation successfully extends its application for the synthesis of phenanthridines and dibenzooxazepines. This new synthetic protocol not only extends the application platform for palladium-catalyzed C-C coupling of aryl halides with isocyanides, but also opens atom-economic and step-economic synthetic routes for nitrogen-containing heterocyclic compounds with wide functional group compatibility. Copyright