Acetamide, N-(4,5-diphenyl-2-oxazolyl)-

Base Information

Chemical Name:Acetamide, N-(4,5-diphenyl-2-oxazolyl)-
CAS No.:35629-39-1
Molecular Formula:C₁₇H₁₄N₂O₂
Molecular Weight:278.31
Hs Code.:2934999090
DSSTox Substance ID:DTXSID30189110
Nikkaji Number:J54.090K
Wikidata:Q83061051
ChEMBL ID:CHEMBL1609102
Mol file:35629-39-1.mol

Synonyms:ACETAMIDE, N-(4,5-DIPHENYL-2-OXAZOLYL)-;35629-39-1;2-Acetamido-4,5-diphenyloxazole;N-(4,5-diphenyl-1,3-oxazol-2-yl)acetamide;Cambridge id 6941581;Oprea1_208337;MLS000677093;CHEMBL1609102;DTXSID30189110;HMS2591O18;STK090299;AKOS002234570;LS-9454;N-(4,5-Diphenyl-2-oxazolyl)acetamide;NCGC00245646-01;SMR000270921;SR-01000246699;SR-01000246699-1;N~1~-(4,5-DIPHENYL-1,3-OXAZOL-2-YL)ACETAMIDE

Suppliers and Price of Acetamide, N-(4,5-diphenyl-2-oxazolyl)-

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

American Custom Chemicals Corporation
N-(4,5-DIPHENYL-1,3-OXAZOL-2-YL)ACETAMIDE 95.00%
5MG
$ 499.85

Total 3 raw suppliers

Chemical Property of Acetamide, N-(4,5-diphenyl-2-oxazolyl)-

Chemical Property:

Refractive Index:1.5500 (estimate)
Boiling Point:421.12°C (rough estimate)
PSA：58.62000
Density:1.214g/cm³
LogP:4.61650
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:278.105527694
Heavy Atom Count:21
Complexity:349

Purity/Quality:

99% ^*data from raw suppliers

N-(4,5-DIPHENYL-1,3-OXAZOL-2-YL)ACETAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=NC(=C(O1)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of Acetamide, N-(4,5-diphenyl-2-oxazolyl)-

There total 5 articles about Acetamide, N-(4,5-diphenyl-2-oxazolyl)- 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:

: 49656-04-4
2-Chlor-4,5-diphenyl-oxazol

: 35629-39-1
N-(4,5-diphenyl-oxazol-2-yl)-acetamide

Guidance literature:: With ammonia; Erhitzen des Reaktionsprodukts mit Acetanhydrid;

Reference yield:

: 5014-83-5
4,5-diphenyloxazol-2-one

: 35629-39-1
N-(4,5-diphenyl-oxazol-2-yl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: POCl₃; triethylamine

2: ethanolic NH₃ / Erhitzen des Reaktionsprodukts mit Acetanhydrid

With ammonia; triethylamine; trichlorophosphate;