(Trifluorosilyl)methyl 2-chlorobenzoate

Base Information

Chemical Name:(Trifluorosilyl)methyl 2-chlorobenzoate
CAS No.:76240-95-4
Molecular Formula:C8H6ClF3O2Si
Molecular Weight:254.668
Hs Code.:
DSSTox Substance ID:DTXSID30504122
Wikidata:Q82358395

Synonyms:(Trifluorosilyl)methyl 2-chlorobenzoate;76240-95-4;DTXSID30504122;(2-chlorobenzoyloxymethyl)trifluorosilane

Suppliers and Price of (Trifluorosilyl)methyl 2-chlorobenzoate

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 (Trifluorosilyl)methyl 2-chlorobenzoate

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:253.9777681
Heavy Atom Count:15
Complexity:234

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(=O)OC[Si](F)(F)F)Cl

Technology Process of (Trifluorosilyl)methyl 2-chlorobenzoate

There total 2 articles about (Trifluorosilyl)methyl 2-chlorobenzoate 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: 85.0%

: 76241-01-5
(2-chlorobenzoyloxymethyl)trimethoxysilane

: 76240-95-4
2(2-chlorobenzoyloxymethyl)trifluorosilane

Guidance literature:: With boron trifluoride diethyl etherate; Heating;

Reference yield:

: 16463-38-0
potassium 2-chlorobenzoate

: 76240-95-4
2(2-chlorobenzoyloxymethyl)trifluorosilane

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / dimethylformamide / Heating

2: 85 percent / BF₃*(C₂H₅)2O / Heating

With boron trifluoride diethyl etherate; In N,N-dimethyl-formamide;