Oxirane, 2-(1-cyclohexen-1-yl)-3-(1-methylethyl)-, (2S,3R)- (9CI)

Base Information

Chemical Name:Oxirane, 2-(1-cyclohexen-1-yl)-3-(1-methylethyl)-, (2S,3R)- (9CI)
CAS No.:697291-75-1
Molecular Formula:C11H18O
Molecular Weight:166.26002
Hs Code.:
Mol file:697291-75-1.mol

Synonyms:Oxirane, 2-(1-cyclohexen-1-yl)-3-(1-methylethyl)-, (2S,3R)- (9CI)

Suppliers and Price of Oxirane, 2-(1-cyclohexen-1-yl)-3-(1-methylethyl)-, (2S,3R)- (9CI)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Oxirane, 2-(1-cyclohexen-1-yl)-3-(1-methylethyl)-, (2S,3R)- (9CI)

Chemical Property:

PSA：12.53000
LogP:2.91020

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

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Technology Process of Oxirane, 2-(1-cyclohexen-1-yl)-3-(1-methylethyl)-, (2S,3R)- (9CI)

There total 2 articles about Oxirane, 2-(1-cyclohexen-1-yl)-3-(1-methylethyl)-, (2S,3R)- (9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: (1R,2R)-1-chloro-1-(cyclohex-1-enyl)-3-methylbutan-2-ol

: 697291-75-1
(2S,3R)-2-(cyclohex-1-enyl)-3-isopropyloxirane

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 25 ℃; for 2h;
DOI:10.1002/ejoc.200300726

Reference yield:

: 329771-08-6
(+)-(1R,2R)-1-(cyclohex-1-enyl)-1-[(S)-N-methyl-S-phenylsulfonimidoyl]-3-methylbutan-2-ol

: 697291-75-1
(2S,3R)-2-(cyclohex-1-enyl)-3-isopropyloxirane

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / CH₂Cl₂ / 2 h / 25 °C

2: 92 percent / DBU / CH₂Cl₂ / 2 h / 25 °C

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane;
DOI:10.1002/ejoc.200300726