37457-15-1

Basic information

• Product Name: 2-Cyclohexen-1-one,2-methyl-3-(2-methylpropoxy)-(9CI)
• Synonyms: 2-Cyclohexen-1-one,2-methyl-3-(2-methylpropoxy)-(9CI)
• CAS NO: 37457-15-1
• Molecular Formula: C₁₁H₁₈O₂
• Molecular Weight: 182.25942
• Product Categories: CYCLOHEXANONE
• Mol File: 37457-15-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 285.9 °C at 760 mmHg
• Flash Point: 118.8 °C
• Appearance: /
• Density: 0.96 g/cm³
• Vapor Pressure: 0.00273mmHg at 25°C
• Refractive Index: 1.465
• CAS DataBase Reference: 2-Cyclohexen-1-one,2-methyl-3-(2-methylpropoxy)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one,2-methyl-3-(2-methylpropoxy)-(9CI)(37457-15-1)
• EPA Substance Registry System: 2-Cyclohexen-1-one,2-methyl-3-(2-methylpropoxy)-(9CI)(37457-15-1)

Safety Data

• Hazardous Substances Data: 37457-15-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H18O2/c1-8(2)7-13-11-6-4-5-10(12)9(11)3/h8H,4-7H2,1-3H3

Upstream product

• 1193-55-1 2-methylcyclohexane-1,3-dione 
• 78-83-1 2-methyl-propan-1-ol 
• 504-02-9 1,3-cylohexanedione 

Downstream Products

• 1122-20-9 2,3-dimethylcyclohex-2-en-1-one 
• 98954-18-8 2-methyl-3-vinyl-cyclohex-2-enone 
• 65093-74-5 (2-methyl-3-oxo-cyclohex-1-enyl)-acetic acid ethyl ester 
• 104190-15-0 3-(3-Furan-2-yl-propyl)-2-methyl-cyclohex-2-enone 
• 81465-60-3 3-isobutoxy-6-isopropyl-2-methyl-2-cyclohexen-1-one 
• 74483-09-3 <2'-(2-Methyl-3-oxocyclohex-1-en-1-yl)ethenylidene>cyclohexane 
• 89998-56-1 3-ethynyl-2-methylcyclohex-2-en-1-one 
• 89998-61-8 14-epi-9,10-secocholesta-5⁽¹⁰⁾,8-dien-6-yn-1-one 
• 89998-62-9 9,10-Secocholesta-5⁽¹⁰⁾,8⁽¹⁴⁾-dien-6-yn-1-one 
• 90079-81-5 (6R)-14-epi-9,10-secocholesta-5⁽¹⁰⁾,6,7-trien-1-one 
• 74398-26-8 (6R)-9,10-secocholesta-5⁽¹⁰⁾,6,7-triene-1-one 
• 73723-49-6 3-isobutoxy-2,6-dimethylcyclohex-2-en-1-one 
• 162087-05-0 2-methyl-4-(tetrahydropyran-2-yloxymethyl)cyclohex-2-enone 
• 441011-26-3 3-(2'-furanyl)-2-methyl-2-cyclohexen-1-one 

Relevant articles and documents

Catalytic enantioselective approach to the eudesmane sesquiterpenoids: Total synthesis of (+)-carissone

(Chemical Equation Presented) A catalytic enantioselective approach to the eudesmane sesquiterpenoids is reported. The strategic use of a palladium-catalyzed enantioselective alkylation of vinylogous ester substrates forged the C(10) all-carbon quaternary

Remarkable effect of aluminum reagents on rearrangements of epoxy acylates via stable cation intermediates and its application to the synthesis of (S)-(+)-sporochnol A

A remarkable effect of (C6F5O)3Al for promoting the rearrangement of epoxy acylates via stable cation intermediates was found, and new methods for constructing chiral benzylic, vinylic, and acetylenic quaternary carbon centers were developed. During the study, the importance of the ionic nature of the O - metal bond in the intermediates of such epoxides was addressed. This method was applied to the asymmetric total synthesis of (S)-(+)-sporochnol A.

Competitive Intramolecular Cycloaddition and Tandem Cycloaddition/-Sigmatropic Rearrangement Sequence of Allenyl 3-Vinyl-2-cyclohexenyl Ethers: Evidence for Switching of the Reaction Pathway by the Substituent Effects

The base-catalyzed intramolecular cycloaddition reactions (t-BuOK, t-BuOH, 83 deg C) of variously substituted propargyl 3-vinyl-2-cyclohexenyl ethers have been investigated.The reaction proceeded smoothly via the initial isomerization to the corresponding