54783-36-7

Basic information

• Product Name: 2-hydroxy-3-(isopropyl)-6-methylcyclohex-2-en-1-one
• Synonyms: 2-hydroxy-3-(isopropyl)-6-methylcyclohex-2-en-1-one;2-Cyclohexen-1-one,2-hydroxy-6-methyl-3-(1-methylethyl)-;2-Hydroxy-3-isopropyl-6-methyl-2-cyclohexene-1-one;2-Hydroxy-6-methyl-3-(1-methylethyl)-2-cyclohexen-1-one;3-Hydroxy-p-mentha-3-ene-2-one;Einecs 259-345-2;2-hydroxy-3-isopropyl-6-methylcyclohex-2-enone
• CAS NO: 54783-36-7
• Molecular Formula: C₁₀H₁₆O₂
• Molecular Weight: 168.23284
• EINECS: 259-345-2
• Mol File: 54783-36-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 285.6°C at 760 mmHg
• Flash Point: 119.9°C
• Appearance: /
• Density: 1.042g/cm³
• Vapor Pressure: 0.000317mmHg at 25°C
• Refractive Index: 1.501
• PKA: 9.29±0.40(Predicted)
• CAS DataBase Reference: 2-hydroxy-3-(isopropyl)-6-methylcyclohex-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxy-3-(isopropyl)-6-methylcyclohex-2-en-1-one(54783-36-7)
• EPA Substance Registry System: 2-hydroxy-3-(isopropyl)-6-methylcyclohex-2-en-1-one(54783-36-7)

Safety Data

• Hazardous Substances Data: 54783-36-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H16O2/c1-6(2)8-5-4-7(3)9(11)10(8)12/h6-7,12H,4-5H2,1-3H3

Upstream product

• 18427-47-9 2,6-Dibromo-2-isopropyl-5-methylcyclohexanone 
• 160168-89-8 (5S)-2-methyl-5-(methylethyl)cyclohexan-1-one 
• 18427-47-9 (5R)-2,6-Dibromo-2-isopropyl-5-methylcyclohexanone 
• 127911-15-3 (5R)-5-isopropyl-2-methylcyclohexanone 
• 10458-14-7 (2R,5S)-menthone 
• 2890-55-3 1-isopropyl-2-oxo-cyclohexanecarboxylic acid ethyl ester 
• 1004-77-9 2-isopropylcyclohexanone 
• 10458-14-7 Menthone 
• 196618-45-8 3-isopropyl-6-methylcyclohex-2-enon-2-yl bromoacetate 
• 15356-60-2 (1S,2R,5S)-(+)-menthol 
• 3391-87-5 l-menthone 
• 17627-49-5 trans-5-methyl-2-(1-methylethyl)cyclohexanone 
• 196618-46-9 dimethyl 6-isopropyl-3-methylcyclohex-2-enon-2-ylphosphonoacetate 
• 490-03-9 2-hydroxy-1-p-menthen-3-one 

Downstream Products

• 71843-50-0 1-p-menthene-2,4-diol-3-one 

Relevant articles and documents

Stereoselective synthesis of (6R)- and (6S)-diosphenol and Ψ-diosphenol

Methods are discussed for the stereoselective synthesis of the (R)-and (S)-enantiomers of the diosphenols (5)-(8) by utilizing the commercially available stereoisomers (9), (12), (23) and (25) of carvone and limonene, respectively, as chiral starting materials.

Synthesis of annulated 4-alkylidenebutenolides from natural occurring diosphenols

Diosphenol (3) and Ψ-diosphenol (4), two constituents of the essential oil from the buchu plant, Borosma betulina (Bartl.), were utilized for the synthesis of the anulated 4-ylidenebutenolides (5) and (6).

Synthesis of a new tautomer of diosphenol (buccocamphor)

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