chloro(N,N-dimethylmethanamine)dihydridoboron

Base Information

Chemical Name:chloro(N,N-dimethylmethanamine)dihydridoboron
CAS No.:5353-44-6
Molecular Formula:C3H11BClN
Molecular Weight:107.391
Hs Code.:
Mol file:5353-44-6.mol

Synonyms:

Suppliers and Price of chloro(N,N-dimethylmethanamine)dihydridoboron

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
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price

Total 5 raw suppliers

Chemical Property of chloro(N,N-dimethylmethanamine)dihydridoboron

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of chloro(N,N-dimethylmethanamine)dihydridoboron

There total 6 articles about chloro(N,N-dimethylmethanamine)dihydridoboron 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:

: 97551-46-7
trimethylamine-trimethylphosphine-diborane⁽⁴⁾

: 64160-46-9
BH₂ClP(CH₃)3

: 5353-44-6
(CH₃)3N*BH₂Cl

: 75-22-9
trimethylamine-borane

: 1898-77-7
trimethylphosphine-borane

Guidance literature:: With hydrogenchloride; In dichloromethane; Anhydrous HCl, -196°C, under N2, then -80°C;

Reference yield:

: tetramethylammonium octahydrotriborate

: (CH₃)3NB₃H₇

: 5353-44-6
(CH₃)3N*BH₂Cl

: 75-22-9
trimethylamine-borane

Guidance literature:: With mercury(I) chloride; trimethylamine; In tetrahydrofuran; vacuum line; condensation of THF onto mixt. of 2 equiv. of borate and 1 equiv. of HgCl2 or Hg2Cl2, warming to room temp., stirring (0.5 h), freezing, condensation of 2.2 equiv. Me3N, stirring (overnight), filtration; not isolated, detd. by (11)B-NMR spectroscopy;
DOI:10.1016/S0020-1693(00)93871-4