Diborane(6), chloro-

Base Information Edit

Chemical Name:Diborane(6), chloro-
CAS No.:17927-57-0
Molecular Formula:B₂ClH₅
Molecular Weight:62.1147
Hs Code.:
DSSTox Substance ID:DTXSID80701301
Wikidata:Q82632906
Mol file:17927-57-0.mol

Synonyms:Diborane(6), chloro-;DTXSID80701301;PUBCHEM_53438436;17927-57-0

Suppliers and Price of Diborane(6), chloro-

Supply Marketing:Edit

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 2 raw suppliers

Chemical Property of Diborane(6), chloro- Edit

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:56.9874630
Heavy Atom Count:3
Complexity:2.8

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

Safty Information:

Pictogram(s): 3
Hazard Codes:3

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:[B][B]Cl

Technology Process of Diborane(6), chloro-

There total 28 articles about Diborane(6), chloro- 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: 73.0%

: pentaborane⁽⁹⁾

: 13701-67-2
diboron tetrachloride

: 17927-57-0
monochlorodiborane

: 1-(dichloroboryl)pentaborane

: 10325-39-0
dichloroborane

: 10294-34-5
boron trichloride

: 19287-45-7
diborane

Guidance literature:: In neat (no solvent); reaction carried out in Pyrex tubes to which Teflon valves had been sealed or in a N2-filled glovebox; reaction of B2Cl4 with excess B5H9 in a 1:3 mole ratio; vessel allowed to warm from -196 ° C to ambient temp., 20 min at ambient temp.,; fractionation, yield of 1-BCl2B5H8 based upon amt. of B2Cl4 employed: 73%, based upon amt. of B5H9 consumed: 95%; small amts. of B2H6, BCl2H, B2H5Cl, also material insufficiently volatileto move into vac. line formed;;