Oxazole, 4,5-dihydro-2,4-diphenyl-5-propyl-, cis-

Base Information

Chemical Name:Oxazole, 4,5-dihydro-2,4-diphenyl-5-propyl-, cis-
CAS No.:100423-09-4
Molecular Formula:C₁₈H₁₉NO
Molecular Weight:265.355
Hs Code.:
DSSTox Substance ID:DTXSID001232654

Synonyms:100423-09-4;Oxazole, 4,5-dihydro-2,4-diphenyl-5-propyl-, cis-;DTXSID001232654

Suppliers and Price of Oxazole, 4,5-dihydro-2,4-diphenyl-5-propyl-, 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 Oxazole, 4,5-dihydro-2,4-diphenyl-5-propyl-, cis-

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:265.146664230
Heavy Atom Count:20
Complexity:326

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCC1C(N=C(O1)C2=CC=CC=C2)C3=CC=CC=C3
Isomeric SMILES:CCC[C@@H]1[C@@H](N=C(O1)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of Oxazole, 4,5-dihydro-2,4-diphenyl-5-propyl-, cis-

There total 8 articles about Oxazole, 4,5-dihydro-2,4-diphenyl-5-propyl-, 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: 94.0%

: 825-60-5
benzimidic acid ethyl ester

: 100423-05-0,100423-06-1,131350-14-6
1-Amino-1-phenyl-pentan-2-ol; hydrochloride

: 100423-09-4,100423-10-7
cis-2,4-diphenyl-5-propyl-2-oxazoline

Guidance literature:: In 1,2-dichloro-ethane; for 24h; Heating;
DOI:10.1246/bcsj.58.1991

Reference yield: 92.0%

: 825-60-5
benzimidic acid ethyl ester

: 100423-05-0,100423-06-1,131350-14-6
1-Amino-1-phenyl-pentan-2-ol; hydrochloride

: 100423-09-4,100423-10-7
trans-2,4-diphenyl-5-propyl-2-oxazoline

Guidance literature:: In 1,2-dichloro-ethane; for 24h; Heating;
DOI:10.1246/bcsj.58.1991

Reference yield:

: 17903-41-2
phenyl(trimethylsilyl)methyl bromide

: 100423-09-4,100423-10-7
cis-2,4-diphenyl-5-propyl-2-oxazoline

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / dimethylformamide / 3 h / 140 °C

2: tetrabutylammonium fluoride / dimethylformamide / 18 h / Ambient temperature

3: 96 percent / 100percent hydrazine hydrate / ethanol / 2 h / Heating

4: 94 percent / 1,2-dichloro-ethane / 24 h / Heating

With tetrabutyl ammonium fluoride; hydrazine hydrate; In ethanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1246/bcsj.58.1991