3-Chloro-3-(trifluoroacetyl)oxolan-2-one

Base Information

Chemical Name:3-Chloro-3-(trifluoroacetyl)oxolan-2-one
CAS No.:69243-05-6
Molecular Formula:C6H4ClF3O3
Molecular Weight:216.5423696
Hs Code.:
DSSTox Substance ID:DTXSID80500957
Mol file:69243-05-6.mol

Synonyms:69243-05-6;3-Chloro-3-(trifluoroacetyl)dihydro-2(3H)-furanone;3-Chloro-3-(trifluoroacetyl)oxolan-2-one;DTXSID80500957

Suppliers and Price of 3-Chloro-3-(trifluoroacetyl)oxolan-2-one

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 3 raw suppliers

Chemical Property of 3-Chloro-3-(trifluoroacetyl)oxolan-2-one

Chemical Property:

PSA：43.37000
LogP:1.04230
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:215.9801062
Heavy Atom Count:13
Complexity:262

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC(=O)C1(C(=O)C(F)(F)F)Cl

Technology Process of 3-Chloro-3-(trifluoroacetyl)oxolan-2-one

There total 1 articles about 3-Chloro-3-(trifluoroacetyl)oxolan-2-one 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:

: 69243-05-6
3-chloro-3-trifluoroacetyl-dihydro-furan-2-one

Guidance literature:: Diketon XIII, SO2Cl2;
DOI:10.1021/jm00189a017

Reference yield:

: 69243-05-6
3-chloro-3-trifluoroacetyl-dihydro-furan-2-one

: 69243-07-8
2-(2-amino-4-trifluoromethyl-thiazol-5-yl)-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HCl, aq. AcOH

2: (i) aq. HCl, (ii) /BRN= 605327/

With hydrogenchloride; acetic acid;
DOI:10.1021/jm00189a017