2-[(Benzenesulfonyl)methyl]cyclohexan-1-ol

Base Information

Chemical Name:2-[(Benzenesulfonyl)methyl]cyclohexan-1-ol
CAS No.:60012-50-2
Molecular Formula:C₁₃H₁₈O₃S
Molecular Weight:254.35
Hs Code.:
DSSTox Substance ID:DTXSID60563000

Synonyms:60012-50-2;2-[(Benzenesulfonyl)methyl]cyclohexan-1-ol;DTXSID60563000

Suppliers and Price of 2-[(Benzenesulfonyl)methyl]cyclohexan-1-ol

Supply Marketing:

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

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Chemical Property of 2-[(Benzenesulfonyl)methyl]cyclohexan-1-ol

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:254.09766561
Heavy Atom Count:17
Complexity:325

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C(C1)CS(=O)(=O)C2=CC=CC=C2)O

Technology Process of 2-[(Benzenesulfonyl)methyl]cyclohexan-1-ol

There total 1 articles about 2-[(Benzenesulfonyl)methyl]cyclohexan-1-ol 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:

: 3112-85-4
methylphenylsulfonate

: 286-20-4
cyclohexane-1,2-epoxide

: 60012-50-2
(2'-hydroxycyclohexyl)phenylsulphonylmethane

Guidance literature:: With n-butyllithium; In tetrahydrofuran;

Reference yield:

: 60012-50-2
(2'-hydroxycyclohexyl)phenylsulphonylmethane

: 2-Benzenesulfonylmethyl-cyclohexanone

Guidance literature:: With jones reagent; In acetone; for 2h;

Reference yield:

: 60012-50-2
(2'-hydroxycyclohexyl)phenylsulphonylmethane

: 3045-98-5
2-methylenecyclohexanone

Guidance literature:: Multi-step reaction with 2 steps

1: Jones reagent / acetone / 2 h

2: DBU / CH₂Cl₂; diethyl ether / 3 h

With jones reagent; 1,8-diazabicyclo[5.4.0]undec-7-ene; In diethyl ether; dichloromethane; acetone;