(1-Nitrocyclohexane-1-sulfonyl)benzene

Base Information

Chemical Name:(1-Nitrocyclohexane-1-sulfonyl)benzene
CAS No.:41774-11-2
Molecular Formula:C12H15NO4S
Molecular Weight:269.321
Hs Code.:
DSSTox Substance ID:DTXSID80516634
Wikidata:Q82378135
Mol file:41774-11-2.mol

Synonyms:41774-11-2;(1-Nitrocyclohexane-1-sulfonyl)benzene;SCHEMBL3288129;DTXSID80516634

Suppliers and Price of (1-Nitrocyclohexane-1-sulfonyl)benzene

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of (1-Nitrocyclohexane-1-sulfonyl)benzene

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:269.07217913
Heavy Atom Count:18
Complexity:395

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)([N+](=O)[O-])S(=O)(=O)C2=CC=CC=C2

Technology Process of (1-Nitrocyclohexane-1-sulfonyl)benzene

There total 4 articles about (1-Nitrocyclohexane-1-sulfonyl)benzene 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: 74.0%

: 6-Benzenesulfonyl-6-nitro-hexan-1-ol

: 41774-11-2
α-nitrocyclohexyl phenyl sulfone

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate;
DOI:10.1021/jo00074a010

Reference yield: 64.0%

: 873-55-2
sodium benzenesulfonate

: 1122-60-7
1-nitrocyclohexane

: 41774-11-2
α-nitrocyclohexyl phenyl sulfone

Guidance literature:: With sodium hydroxide; sodium persulfate; potassium hexacyanoferrate(III); In 1,4-dioxane; at 25 ℃; for 0.25h;
DOI:10.1021/jo00210a600