1350468-10-8

Basic information

• Product Name: 3-methyl-1-tosyl-3-vinylpyrrolidine
• Synonyms: 3-methyl-1-tosyl-3-vinylpyrrolidine
• CAS NO: 1350468-10-8
• Molecular Weight: 265.376
• Mol File: 1350468-10-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-methyl-1-tosyl-3-vinylpyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-1-tosyl-3-vinylpyrrolidine(1350468-10-8)
• EPA Substance Registry System: 3-methyl-1-tosyl-3-vinylpyrrolidine(1350468-10-8)

Safety Data

• Hazardous Substances Data: 1350468-10-8(Hazardous Substances Data)

Upstream product

• 57253-30-2 tiglyl bromide 
• 98-59-9 p-toluenesulfonyl chloride 
• 80-59-1 Tiglic acid 
• 1350468-27-7 (E)-N-(2-bromoethyl)-4-methyl-N-(2-methylbut-2-en-1-yl)benzenesulfonamide 
• 497-02-9 (E)-2-methyl-2-buten-1-ol 
• 14316-14-4 N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide 
• 13201-46-2 2-methylbut-2-enoic acid 
• 86410-99-3 N-<(E)-2-methyl-2-butenyl>-p-tosylamide 
• 18303-04-3 N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide 
• 1350468-09-5 (E)-N-(2-iodoethyl)-4-methyl-N-(2-methylbut-2-en-1-yl)benzenesulfonamide 
• 1350468-26-6 (E)-tert-butyl (2-methylbut-2-en-1-yl)(tosyl)carbamate 

Relevant articles and documents

Nickel-Catalyzed Mizoroki–Heck-Type Reactions of Unactivated Alkyl Bromides

The development of a general, nickel-catalyzed alkyl-Mizoroki–Heck reaction of unactivated alkyl bromides is described. The mild reaction proceeds efficiently using a wide range of primary and secondary alkyl bromides, and examples of intermolecular cross

Water control over the chemoselectivity of a Ti/Ni multimetallic system: Heck- or reductive-type cyclization reactions of alkyl iodides

A versatile Ti/Ni multimetallic protocol is described for the efficient catalysis of two different reactions, namely a Heck- and reductive-type cyclization of alkyl iodides, in the absence or presence of water, respectively. Noteworthy, the versatility of