2-[4-(2-[1,1'-Biphenyl]-4-ylvinyl)phenyl]-5-tert-butylbenzoxazole

Base Information

Chemical Name:2-[4-(2-[1,1'-Biphenyl]-4-ylvinyl)phenyl]-5-tert-butylbenzoxazole
CAS No.:16143-18-3
Molecular Formula:C31H27 N O
Molecular Weight:429.561
Hs Code.:2934999090
European Community (EC) Number:240-297-6
Nikkaji Number:J60.807F
Mol file:16143-18-3.mol

Synonyms:2-[4-(2-[1,1'-biphenyl]-4-ylvinyl)phenyl]-5-tert-butylbenzoxazole;NS00055290

Suppliers and Price of 2-[4-(2-[1,1'-Biphenyl]-4-ylvinyl)phenyl]-5-tert-butylbenzoxazole

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 4 raw suppliers

Chemical Property of 2-[4-(2-[1,1'-Biphenyl]-4-ylvinyl)phenyl]-5-tert-butylbenzoxazole

Chemical Property:

Boiling Point:573.3°Cat760mmHg
Flash Point:250.6°C
PSA：26.03000
Density:1.13g/cm³
LogP:8.62970
XLogP3:9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:429.209264485
Heavy Atom Count:33
Complexity:628

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)C=CC4=CC=C(C=C4)C5=CC=CC=C5
Isomeric SMILES:CC(C)(C)C1=CC2=C(C=C1)OC(=N2)C3=CC=C(C=C3)/C=C/C4=CC=C(C=C4)C5=CC=CC=C5

Technology Process of 2-[4-(2-[1,1'-Biphenyl]-4-ylvinyl)phenyl]-5-tert-butylbenzoxazole

There total 4 articles about 2-[4-(2-[1,1'-Biphenyl]-4-ylvinyl)phenyl]-5-tert-butylbenzoxazole 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:

: 51357-73-4
1-([1,1'-biphenyl]-4-yl)-N-phenylmethanimine

: 10127-84-1
5-tert-butyl-2-p-tolylbenzo[d]oxazole

: 16143-18-3
2-[4-(trans-2-biphenyl-4-yl-vinyl)-phenyl]-5-tert-butyl-benzooxazole

Guidance literature:: With potassium hydroxide; In N,N-dimethyl-formamide; at 60 - 65 ℃;
DOI:10.1002/hlca.19670500318

Reference yield:

: 99-94-5
p-Toluic acid

: 16143-18-3
2-[4-(trans-2-biphenyl-4-yl-vinyl)-phenyl]-5-tert-butyl-benzooxazole

Guidance literature:: Multi-step reaction with 2 steps

1: H₃BO₃

2: KOH / dimethylformamide / 60 - 65 °C

With potassium hydroxide; boric acid; In N,N-dimethyl-formamide;
DOI:10.1002/hlca.19670500318

Reference yield:

: 1199-46-8
2-amino-4-tert-butylphenol

: 16143-18-3
2-[4-(trans-2-biphenyl-4-yl-vinyl)-phenyl]-5-tert-butyl-benzooxazole

Guidance literature:: Multi-step reaction with 2 steps

1: H₃BO₃

2: KOH / dimethylformamide / 60 - 65 °C

With potassium hydroxide; boric acid; In N,N-dimethyl-formamide;
DOI:10.1002/hlca.19670500318