1-Cyclohexyl-2-azetidinone

Base Information

Chemical Name:1-Cyclohexyl-2-azetidinone
CAS No.:34094-39-8
Molecular Formula:C9H15NO
Molecular Weight:153.224
Hs Code.:
DSSTox Substance ID:DTXSID10487000

Synonyms:1-cyclohexyl-2-azetidinone;34094-39-8;cyclohexylazetidinone;1-cyclohexyl-azetidin-2-one;SCHEMBL4605352;DTXSID10487000;AKOS015907499

Suppliers and Price of 1-Cyclohexyl-2-azetidinone

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 1-Cyclohexyl-2-azetidinone

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:153.115364102
Heavy Atom Count:11
Complexity:161

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)N2CCC2=O

Technology Process of 1-Cyclohexyl-2-azetidinone

There total 12 articles about 1-Cyclohexyl-2-azetidinone 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: 80.0%

: 77648-12-5
N-Cyclohexyl-Δ¹-azetinium Perchlorate

: 34094-39-8
N-cyclohexyl-2-Azetidinone

Guidance literature:: With pyridine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 ℃; for 0.666667h;
DOI:10.1021/jo00328a001

Reference yield: 78.0%

: 930-21-2
2-azetidinone

: 98-89-5
Cyclohexanecarboxylic acid

: 34094-39-8
N-cyclohexyl-2-Azetidinone

Guidance literature:: With copper(I) thiophene-2-carboxylate; (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(5-methyl-2-(4-fluorophenyl)pyridine(-1H))-iridium(III) hexafluorophosphate; N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; bathophenanthroline; iodomesitylene diacetate; In 1,4-dioxane; at 20 ℃; for 1h; regioselective reaction; Inert atmosphere; Irradiation;
DOI:10.1038/s41586-018-0234-8