N'-(Butan-2-yl)-N,N-dimethyl-1-phenylboranediamine

Base Information

Chemical Name:N'-(Butan-2-yl)-N,N-dimethyl-1-phenylboranediamine
CAS No.:79867-01-9
Molecular Formula:C₁₂H₂₁BN₂
Molecular Weight:204.123
Hs Code.:
DSSTox Substance ID:DTXSID70508341

Synonyms:79867-01-9;N'-(Butan-2-yl)-N,N-dimethyl-1-phenylboranediamine;DTXSID70508341

Suppliers and Price of N'-(Butan-2-yl)-N,N-dimethyl-1-phenylboranediamine

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 N'-(Butan-2-yl)-N,N-dimethyl-1-phenylboranediamine

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:204.1797788
Heavy Atom Count:15
Complexity:167

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:B(C1=CC=CC=C1)(NC(C)CC)N(C)C

Technology Process of N'-(Butan-2-yl)-N,N-dimethyl-1-phenylboranediamine

There total 1 articles about N'-(Butan-2-yl)-N,N-dimethyl-1-phenylboranediamine 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: 75.0%

: 33966-50-6
SEC-BUTYLAMINE

: 1196-44-7
chloro(dimethylamino)phenylborane

: 79867-01-9
s-butylaminodimethylaminophenylborane

Guidance literature:: With triethylamine; In benzene; byproducts: NEt4Cl; B-compd. dissolved in benzene, cooled in ice bath, s-butylamine dissolved in benzene added dropwise with stirring, mixt. allowed to attain roomtemp., triethylamine added to resulted complex, mixt. refluxed for 3 h; NEt4Cl filtered, solvent removed from the filtrate, residue vac. distd.; elem. anal.;
DOI:10.1016/S0022-328X(00)93444-2