5-Benzyl-3-phenylisoxazole

Base Information

Chemical Name:5-Benzyl-3-phenylisoxazole
CAS No.:18753-56-5
Molecular Formula:C16H13NO
Molecular Weight:235.285
Hs Code.:
Mol file:18753-56-5.mol

Synonyms:5-Benzyl-3-phenylisoxazol;Isoxazole,5-benzyl-3-phenyl;5-Benzyl-3-phenylisoxazole;3-Phenyl-5-benzyl-isoxazol;

Suppliers and Price of 5-Benzyl-3-phenylisoxazole

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 5-Benzyl-3-phenylisoxazole

Chemical Property:

PSA：26.03000
LogP:3.93240

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 5-Benzyl-3-phenylisoxazole

There total 14 articles about 5-Benzyl-3-phenylisoxazole 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: 99.0%

: 18753-56-5
3-Phenyl-5-(phenylmethyl)isoxazole

Guidance literature:

Reference yield: 90.0%

: 10147-11-2
propargyl benzene

: 932-90-1
Benzaldoxime

: 18753-56-5
3-Phenyl-5-(phenylmethyl)isoxazole

Guidance literature:: Benzaldoxime; With N-chloro-succinimide; TPGS-750-M; In water; at 20 ℃; for 4h;

propargyl benzene; With triethylamine; In water; at 20 ℃; for 8h;

Reference yield: 86.0%

: 886-66-8
1,4-diphenyl-1,3-butadiyne

: 18753-56-5
3-Phenyl-5-(phenylmethyl)isoxazole

Guidance literature:: With hydroxylamine hydrochloride; triethylamine; In dimethyl sulfoxide; at 110 ℃; for 20h; sealed flask;
DOI:10.1021/ol300872e