2-Azetidinone, 1,3,4-triphenyl-, cis-

Base Information

Chemical Name:2-Azetidinone, 1,3,4-triphenyl-, cis-
CAS No.:16141-50-7
Molecular Formula:C₂₁H₁₇NO
Molecular Weight:299.372
Hs Code.:
DSSTox Substance ID:DTXSID80426340
Nikkaji Number:J1.141.160F
Wikidata:Q82239277
Mol file:16141-50-7.mol

Synonyms:2-Azetidinone, 1,3,4-triphenyl-, cis-;MLS002666906;DTXSID80426340;cis-1,3,4-triphenyl-2-azetidinone;1,3beta,4beta-Triphenylazetidine-2-one;16141-50-7;SMR001554458

Suppliers and Price of 2-Azetidinone, 1,3,4-triphenyl-, cis-

Supply Marketing:

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

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Chemical Property of 2-Azetidinone, 1,3,4-triphenyl-, cis-

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:299.131014166
Heavy Atom Count:23
Complexity:402

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2C(N(C2=O)C3=CC=CC=C3)C4=CC=CC=C4
Isomeric SMILES:C1=CC=C(C=C1)[C@H]2[C@H](N(C2=O)C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of 2-Azetidinone, 1,3,4-triphenyl-, cis-

There total 19 articles about 2-Azetidinone, 1,3,4-triphenyl-, cis- 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: 89.0%

: 103-82-2
phenylacetic acid

: 538-51-2
benzylidene phenylamine

: 7477-20-5,16141-49-4,16141-50-7,31467-82-0,76455-34-0
(±)-cis-1,3,4-triphenylazetidin-2-one

Guidance literature:: With oxalyl dichloride; 2,3-bis(4-methoxyphenyl)cyclopropenone; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; for 4.25h; diastereoselective reaction; Reflux;
DOI:10.1016/j.tetlet.2016.10.012

Reference yield: 83.0%

: 538-51-2
benzylidene phenylamine

: 3282-32-4
2-diazo-acetophenone

: 16141-49-4
trans-1,3,4-triphenyl-2-azetidinone

: 7477-20-5,16141-49-4,16141-50-7,31467-82-0,76455-34-0
(±)-cis-1,3,4-triphenylazetidin-2-one

Guidance literature:: In 5,5-dimethyl-1,3-cyclohexadiene; at 140 ℃; for 12h; stereoselective reaction;
DOI:10.1080/00397911.2017.1378358

Reference yield: 77.0%

: 536-74-3
phenylacetylene

: 1137-96-8,26505-49-7,201024-81-9
N-(benzylidene)aniline N-oxide

: 7477-20-5,16141-49-4,16141-50-7,31467-82-0,76455-34-0
(±)-cis-1,3,4-triphenylazetidin-2-one

Guidance literature:: With copper(II) ferrite; water; diethylamine; In acetonitrile; at 20 ℃; for 18h; Solvent; Reagent/catalyst; Time; Temperature; stereoselective reaction; Catalytic behavior;
DOI:10.1039/d0nj02660c