(1,1-Dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene

Base Information

Chemical Name:(1,1-Dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene
CAS No.:103670-60-6
Molecular Formula:C9H5Br2F3
Molecular Weight:329.942
Hs Code.:
DSSTox Substance ID:DTXSID80546597
Nikkaji Number:J909.723F
Mol file:103670-60-6.mol

Synonyms:103670-60-6;(1,1-Dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene;DTXSID80546597;1,1-dibromo-2-phenyl-3,3,3-trifluoropropene

Suppliers and Price of (1,1-Dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene

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 1 raw suppliers

Chemical Property of (1,1-Dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:329.86896
Heavy Atom Count:14
Complexity:223

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=C(Br)Br)C(F)(F)F

Technology Process of (1,1-Dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene

There total 2 articles about (1,1-Dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene 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: 92.0%

: 558-13-4
carbon tetrabromide

: 434-45-7
2,2,2-Trifluoroacetophenone

: 103670-60-6
(1,1-dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene

Guidance literature:: With triphenylphosphine; In dichloromethane; at -40 - 20 ℃;
DOI:10.1039/c39910000566

Reference yield:

: 594-15-0
chlorotribromomethane

: 434-45-7
2,2,2-Trifluoroacetophenone

: 103670-60-6
(1,1-dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene

: ((Z)-2-Bromo-2-chloro-1-trifluoromethyl-vinyl)-benzene

: ((E)-2-Bromo-2-chloro-1-trifluoromethyl-vinyl)-benzene

Guidance literature:: With triphenylphosphine; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; 1.) CH₂Cl₂, -40 deg C, 30 min, 2.) CH₂Cl₂, from -40 deg C to RT, overnight;

Reference yield: 80.0%

: 15206-55-0
methyl 2-oxo-2-phenylacetate

: 103670-60-6
(1,1-dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene

: methyl 3-bromo-5,5,5-trifluoro-2-hydroxy-2,4-diphenyl-3-pentenoate

Guidance literature:: (1,1-dibromo-3,3,3-trifluoroprop-1-en-2-yl)benzene; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;

methyl 2-oxo-2-phenylacetate; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
DOI:10.1246/bcsj.72.1365