55234-03-2

Basic information

• Product Name: Cyclohexanone, 2-bromo-2,6-dimethyl-
• CAS NO: 55234-03-2
• Molecular Formula: C8H13BrO
• Molecular Weight: 205.095
• Mol File: 55234-03-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-bromo-2,6-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-bromo-2,6-dimethyl-(55234-03-2)
• EPA Substance Registry System: Cyclohexanone, 2-bromo-2,6-dimethyl-(55234-03-2)

Safety Data

• Hazardous Substances Data: 55234-03-2(Hazardous Substances Data)

Upstream product

• 29800-80-4 2,6-dimethyl-1-<(trimethylsilyl)oxy>cyclohexene 
• 63547-53-5 2,6-dimethyl-1-(trimethylsiloxy)cyclohexene 
• 766-43-8 trans-2,6-dimethylcyclohexanone 
• 2816-57-1 2,6-dimethylcyclohexanone 

Downstream Products

• 123992-61-0 ethyl (ξ-acetoxy-2,6β-dimethyl-2-cyclohexen-1-yl)acetate 
• 123992-76-7 3-(diazoacetonylidene)-2,4-dimethyl-1-cyclohexene 
• 123992-72-3 ethyl (2,6-dimethyl-2-cyclohexen-1-ylidene)acetate 
• 123992-58-5 (2,6-dimethyl-2-cyclohexen-1-ylidene)acetic acid 
• 126754-17-4 (1RS,5SR,8aRS)-1-(3-furyl)-5,8a-dimethyl-1,5,6,7,8,8a-hexahydro-3H-2-benzopyran-3-one 
• 136587-15-0 (2RS,6RS)-2-<3-furyloxomethyl>-2,6-dimethylcyclohexanone 
• 136587-16-1 (2RS,6SR)-2-<3-furylhydroxomethyl>-2,6-dimethylcyclohexanone 
• 136587-26-3 (1RS,4SR,8aRS)-2-(3-furyl)-5,8a-dimethyl-4-(benzylseleno)-3,4,6,7,8,8a-hexahydro-1H-2-benzopyran-3-one 
• 136587-27-4 (1RS,5RS,8aRS)-1-(3-furyl)-5,8a-dimethyl-5-(benzylseleno)-1,5,6,7,8,8a-hexahydro-3H-2-benzopyran-3-one 
• 52730-12-8 dl-pyroangolensolide 
• 40790-56-5 2,6-dimethyl-2-cyclohexen-1-one 
• 2570-68-5 6-oxo-2-methyl-heptanoic acid 
• 88974-48-5 1,5-dimethyl-6,8-dioxabicyclo[3.2.1]octan-7-one 
• 66633-36-1 2-hydroxy-2,6-dimethylcyclohexanone 

Relevant articles and documents

A New, General Cyclopentenone Synthesis

A new synthesis of cyclopentenones, involving an Rh(II)-catalyzed, intramolecular carbon-hydrogen insertion of diazomethyl ketones derived from α,β-unsaturated acids, is described.

Oxidation of Enol Silyl Ethers: Preparation of Aeginetolide, Dihydroactinidiolide, and Actinidiolide

The preparation of the C11-terpenic lactones aeginetolide (1), dihydroactinidiolide (2), and actinidiolide (3) by using 1,3,3-trimethyl-2-(trimethylsiloxy)cyclohexene (9) as a common precursor is discussed.The key steps in the synthetic route involve the sequential m-chloroperbenzoic acid (MCPBA) oxidation and acetylation of 9 and of the siloxy diene 13 derived from 9.