1196-73-2

Basic information

• Product Name: 1-Cyclohexen-1-ol, 2-methyl-, acetate
• CAS NO: 1196-73-2
• Molecular Formula: C9H14O2
• Molecular Weight: 154.209
• Mol File: 1196-73-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Cyclohexen-1-ol, 2-methyl-, acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Cyclohexen-1-ol, 2-methyl-, acetate(1196-73-2)
• EPA Substance Registry System: 1-Cyclohexen-1-ol, 2-methyl-, acetate(1196-73-2)

Safety Data

• Hazardous Substances Data: 1196-73-2(Hazardous Substances Data)

Usage

Physical state

colorless liquid

Uses

flavoring and fragrance ingredient, added to perfumes, soaps, and lotions, production of flavors for food and beverages, manufacturing of pharmaceuticals and other consumer products

Properties

fruity, floral odor, versatile chemical properties

Synthesized from

1-Cyclohexen-1-ol, 2-methyl-

Upstream product

• 557-99-3 acetyl fluoride 
• 19980-35-9 1-trimethylsilyloxy-2-methyl-1-cyclohexene 
• 64-19-7 acetic acid 
• 583-60-8 2-Methylcyclohexanone 
• 75-36-5 acetyl chloride 
• 563-63-3 silver(I) acetate 
• 108-94-1 cyclohexanone 
• 21750-52-7 1-tri-n-butylstannyloxy-2-methylcyclohex-1-ene 
• 17851-97-7 1-tri(n-butyl)stannyloxy-1-cyclohexene 
• 108-24-7 acetic anhydride 

Downstream Products

• 16178-87-3 2-methyl-2-allylcyclohexanone 
• 80594-90-7 cis-6-methyl-2-nitrocyclohexanone 
• 80594-88-3 trans-6-methyl-2-nitrocyclohexanone 
• 110350-06-6 4-Nitro-benzenesulfonic acid 1-methyl-2-oxo-cyclohexyl ester 
• 3128-07-2 6-oxoheptanoic acid 
• 80594-87-2 2-methyl-2-nitrocyclohexan-1-one 
• 1121-18-2 2-methyl-2-cyclohexen-1-one 
• 22554-27-4 (S)-2-methylcyclohexanone 
• 22554-29-6 (R)-2-methylcyclohexanone 
• 137639-98-6 2,2'-Dimethyl-bicyclohexyl-3,3'-dione 
• 583-60-8 2-Methylcyclohexanone 
• 67301-11-5 (E)-1-methyl-2-oxocyclohexane-2-propenoic acid methyl ester 
• 67301-13-7 (Z)-1-methyl-2-oxocyclohexane-2-propenoic acid methyl ester 
• 17206-52-9 2-ethyl-2-methyl-cyclohexanone 

Relevant articles and documents

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Unprecedented Route to Enolates from Silyl Enol Ethers and Enol Acetates: Reaction with Hard and Soft Electrophiles

Reaction of silyl enol ethers with lithium, sodium or better, potassium alkoxides resulted in a rapid formation of enolates which were trapped with hard electrophiles and benzaldehyde.Moreover, in the aldolisation reaction, only a catalytic amount of alka

REGIOSPECIFIC SYNTHESIS OF α-ARYLSULFONOXY KETONES FROM KETONE DERIVATIVES

Isomeric enol ester, enamine, and silyl enol ether derivatives of unsymmetrical ketones are converted regiospecifically to α-arylsulfonoxy ketones with arylsulfonyl peroxides.