5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydro-1,2-oxazole

Base Information

Chemical Name:5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydro-1,2-oxazole
CAS No.:93665-81-7
Molecular Formula:C7H8F3NO
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID80542519

Synonyms:93665-81-7;5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydroisoxazole;DTXSID80542519;5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydro-1,2-oxazole

Suppliers and Price of 5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydro-1,2-oxazole

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydro-1,2-oxazole

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:179.05579836
Heavy Atom Count:12
Complexity:231

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=C)C1CC(=NO1)C(F)(F)F

Technology Process of 5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydro-1,2-oxazole

There total 1 articles about 5-(Prop-1-en-2-yl)-3-(trifluoromethyl)-4,5-dihydro-1,2-oxazole 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:

: 14533-30-3
Trifluoroacetohydroximoyl bromide etherate

: 78-79-5,9003-31-0
isoprene

: 100695-97-4
(E)-1,1,1-Trifluoro-4-methyl-hexa-3,5-dien-2-one oxime

: 93665-82-8
5-Methyl-3-trifluoromethyl-5-vinyl-4,5-dihydro-isoxazole

: 93665-81-7
5-Isopropenyl-3-trifluoromethyl-4,5-dihydro-isoxazole

Guidance literature:: With triethylamine; In diethyl ether; for 4h; Yield given. Yields of byproduct given; Ambient temperature;
DOI:10.1246/bcsj.58.2061