tris(2-chloro phenyl)boroxine

Base Information

Chemical Name:tris(2-chloro phenyl)boroxine
CAS No.:79422-00-7
Molecular Formula:C₁₈H₁₂B₃Cl₃O₃
Molecular Weight:415.083
Hs Code.:

Synonyms:tris(2-chloro phenyl)boroxine

Suppliers and Price of tris(2-chloro phenyl)boroxine

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 tris(2-chloro phenyl)boroxine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tris(2-chloro phenyl)boroxine

There total 6 articles about tris(2-chloro phenyl)boroxine 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:

: 3900-89-8
2-Chlorobenzeneboronic acid

: 79422-00-7
tris(2-chloro phenyl)boroxine

Guidance literature:: With sulfuric acid;
DOI:10.1021/ja01319a053

Reference yield:

: 36692-27-0
2-chlorophenylmagnesium bromide

: 688-74-4
boric acid tributyl ester

: 79422-00-7
tris(2-chloro phenyl)boroxine

Guidance literature:: In diethyl ether; byproducts: H2O; synthesis of dihydroxy borane at -75°C in ether, dehydration by heating in vac. to 80°C (12h), then to 110°C (4h);;
DOI:10.1021/ja01350a045

Reference yield:

: 36692-27-0
2-chlorophenylmagnesium bromide

: 79422-00-7
tris(2-chloro phenyl)boroxine

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / und anschliessenden Hydrolyse

2: beim Erhitzen

With diethyl ether;
DOI:10.1021/ja01319a053