29342-27-6

Basic information

• Product Name: 2-Butanone, 4-(benzoyloxy)-
• CAS NO: 29342-27-6
• Molecular Formula: C11H12O3
• Molecular Weight: 192.214
• Mol File: 29342-27-6.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 2-Butanone, 4-(benzoyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butanone, 4-(benzoyloxy)-(29342-27-6)
• EPA Substance Registry System: 2-Butanone, 4-(benzoyloxy)-(29342-27-6)

Safety Data

• Hazardous Substances Data: 29342-27-6(Hazardous Substances Data)

Upstream product

• 590-90-9 1-Hydroxy-3-butanone 
• 98-88-4 benzoyl chloride 
• 5205-12-9 3-methylbut-3-enyl benzoate 
• 18203-32-2 3-butenyl benzoate 
• 78-94-4 methyl vinyl ketone 
• 65-85-0 benzoic acid 
• 122471-85-6 3-butynyl benzoate 
• 136-60-7 benzoic acid, butyl ester 
• 536-80-1 iodosylbenzene 

Downstream Products

• 78840-60-5 Benzoic acid 3-((2S,5S)-2,5-dimethoxy-1,4-dimethyl-3,6-dioxo-piperazin-2-yl)-but-3-enyl ester 
• 78840-59-2 Benzoic acid (E)-3-((2S,5S)-2,5-dimethoxy-1,4-dimethyl-3,6-dioxo-piperazin-2-yl)-but-2-enyl ester 
• 569678-68-8 3,3-difluorobutyl benzoate 
• 78-94-4 methyl vinyl ketone 
• 65-85-0 benzoic acid 
• 78840-58-1 Benzoic acid 3-((2S,5S)-2,5-dimethoxy-1,4-dimethyl-3,6-dioxo-piperazin-2-yl)-3-hydroxy-butyl ester 

Relevant articles and documents

Gold N-Heterocyclic Carbene Catalysts for the Hydrofluorination of Alkynes Using Hydrofluoric Acid: Reaction Scope, Mechanistic Studies and the Tracking of Elusive Intermediates

An efficient and chemoselective methodology deploying gold-N-heterocyclic carbene (NHC) complexes as catalysts in the hydrofluorination of terminal alkynes using aqueous HF has been developed. Mechanistic studies shed light on an in situ generated catalyst, formed by the reaction of Br?nsted basic gold pre-catalysts with HF in water, which exhibits the highest reactivity and chemoselectivity. The catalytic system has a wide alkyl substituted-substrate scope, and stoichiometric as well as catalytic reactions with tailor-designed gold pre-catalysts enable the identification of various gold species involved along the catalytic cycle. Computational studies aid in understanding the chemoselectivity observed through examination of key mechanistic steps for phosphine- and NHC-coordinated gold species bearing the triflate counterion and the elusive key complex bearing a bifluoride counterion.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

A compound of Formula I, including pharmaceutically acceptable salts thereof, and compositions and methods for treating human immunodeficiency virus (HIV) infection are set forth: (I)

Tuning Regioselectivity of Wacker Oxidation in One Catalytic System: Small Change Makes Big Step

A regioselectivity switchable aerobic Wacker-Tsuji oxidation has been developed using catalytic tert-butyl nitrite as a simple organic redox cocatalyst. By solely switching the solvent, either substituted aldehydes or ketones could be prepared under mild