2-Azetidinone, 3-azido-1,4-diphenyl-, cis-

Base Information

Chemical Name:2-Azetidinone, 3-azido-1,4-diphenyl-, cis-
CAS No.:16311-94-7
Molecular Formula:C15H12N4O
Molecular Weight:264.286
Hs Code.:
DSSTox Substance ID:DTXSID50484033
Nikkaji Number:J3.605.775K

Synonyms:2-Azetidinone, 3-azido-1,4-diphenyl-, cis-;DTXSID50484033;16311-94-7

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

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-Azetidinone, 3-azido-1,4-diphenyl-, cis-

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:264.10111102
Heavy Atom Count:20
Complexity:406

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2C(C(=O)N2C3=CC=CC=C3)N=[N+]=[N-]
Isomeric SMILES:C1=CC=C(C=C1)[C@@H]2[C@@H](C(=O)N2C3=CC=CC=C3)N=[N+]=[N-]

Technology Process of 2-Azetidinone, 3-azido-1,4-diphenyl-, cis-

There total 6 articles about 2-Azetidinone, 3-azido-1,4-diphenyl-, 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: 91.0%

: 18523-48-3
2-azidoacetic acid

: 538-51-2
benzylidene phenylamine

: 16311-94-7
cis-3-azido-1,4-diphenylazetidin-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