514848-29-4

Basic information

• Product Name: 2-Butanone, 4-(2-propenylthio)- (9CI)
• Synonyms: 2-Butanone, 4-(2-propenylthio)- (9CI)
• CAS NO: 514848-29-4
• Molecular Formula: C7H12OS
• Molecular Weight: 144.23458
• Product Categories: ACETYLGROUP
• Mol File: 514848-29-4.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Butanone, 4-(2-propenylthio)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butanone, 4-(2-propenylthio)- (9CI)(514848-29-4)
• EPA Substance Registry System: 2-Butanone, 4-(2-propenylthio)- (9CI)(514848-29-4)

Safety Data

• Hazardous Substances Data: 514848-29-4(Hazardous Substances Data)

Upstream product

• 78-94-4 methyl vinyl ketone 
• 107-05-1 3-chloroprop-1-ene 
• 106-95-6 allyl bromide 
• 2547-92-4 S-allylisothiourea hydrochloride 
• 870-23-5 prop-2-ene-1-thiol 

Relevant articles and documents

Photo-Biocatalytic Cascades for the Synthesis of Volatile Sulfur Compounds and Chemical Building Blocks

Biocatalysis is a branch of catalysis that exploits enzymes to perform highly stereoselective chemical transformations under mild and sustainable conditions. This Synpact highlights how biocatalysis can be used in the synthesis of chiral 1,3-mercaptoalkan

N-heterocyclic carbene catalyzed carba-, sulfa-, and phospha-Michael additions with NHC·CO2 adducts as precatalysts

N-heterocyclic carbene catalyzed Michael additions have been revisited with 1,3-dialkyl- or 1,3-diarylimidazol(in)ium-2-carboxylates, that is, NHC·CO2 adducts, as the source of the free NHC catalysts in solution. Using these precatalysts, a number of efficient carba-, sulfa-, and phospha-Michael additions were achieved very conveniently, without the need for an external strong base to generate the NHC by deprotonation of an azolium salt. To further expand the scope of the procedure, some NHC-catalyzed sulfa-Michael/aldol organocascades were also investigated.

Ceric ammonium nitrate (CAN) as a green and highly efficient promoter for the 1,4-addition of thiols and benzeneselenol to α,β-unsaturated ketones

A mild and efficient process for the 1,4-addition of thiols and benzeneselenols to various α,β-unsaturated ketones using a catalytic amount of CAN with excellent product yields is described. This inexpensive, nontoxic, and readily available catalytic ceric(IV) ammonium nitrate system efficiently catalyzes conjugate addition reactions between thiol derivatives and various α,β-unsaturated ketones under solvent-free conditions. A plausible mechanism for the role of CAN, both as a promoter in free radical chain addition reactions as well as a catalyst for the conjugate addition process is proposed.