151251-52-4

Basic information

• Product Name: 2-[1-[(4-methylphenyl)sulfonyl]tetrahydro-4(1H)-pyridinyliden]ethyl acetate
• Synonyms: 2-[1-[(4-methylphenyl)sulfonyl]tetrahydro-4(1H)-pyridinyliden]ethyl acetate
• CAS NO: 151251-52-4
• Molecular Weight: 323.413
• Mol File: 151251-52-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-[1-[(4-methylphenyl)sulfonyl]tetrahydro-4(1H)-pyridinyliden]ethyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[1-[(4-methylphenyl)sulfonyl]tetrahydro-4(1H)-pyridinyliden]ethyl acetate(151251-52-4)
• EPA Substance Registry System: 2-[1-[(4-methylphenyl)sulfonyl]tetrahydro-4(1H)-pyridinyliden]ethyl acetate(151251-52-4)

Safety Data

• Hazardous Substances Data: 151251-52-4(Hazardous Substances Data)

Upstream product

• 2181-21-7 1-[(4-methylbenzene)sulfonyl]-4-methylidenepiperidine 
• 25260-60-0 cis-1,4-bis(acetyloxy)but-2-ene 
• 1576-98-3 1,4-diacetoxybut-2-ene 
• 33439-27-9 N-tosyl-4-piperidone 
• 108-24-7 acetic anhydride 

Downstream Products

• 1161828-04-1 4-ethyl-1-tosyl-4-vinylpiperidine 
• 151251-57-9 Acetic acid 10-oxo-3-(toluene-4-sulfonyl)-13-oxa-3-aza-dispiro[5.0.5.2]tetradeca-8,11-dien-14-ylmethyl ester 

Relevant articles and documents

Complexes of ruthenum, method for their preparation, and their application in olefin metathesis reactions

The present invention provides new ruthenium complexes of Formula (1), which contain a chelate ring created by a halogen atom X. The invention concerns also a method for the preparation of the new ruthenium complexes and their application in metathesis re

In situ generation of novel acyclic diaminocarbene-copper complex

A novel acyclic diaminocarbene-copper complex appears to be generated from a chloroamidinium salt and Cu(i)-thiophenecarboxylate in the presence of Grignard reagent based on 13C NMR studies and is a highly efficient catalyst for SN2′

Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: Enhancement of catalyst activity through electronic activation

The design, synthesis, stability, and catalytic activity of nitro-substituted Hoveyda-Grubbs metathesis catalysts are described. The highly active and stable meta- and para-substituted complexes are attractive from a practical point of view. These catalys