Phosphinic chloride, dibutyl-

Base Information

Chemical Name:Phosphinic chloride, dibutyl-
CAS No.:683-16-9
Molecular Formula:C8H18ClOP
Molecular Weight:196.657
Hs Code.:
DSSTox Substance ID:DTXSID60382753
Nikkaji Number:J1.174.731K
Wikidata:Q82174162

Synonyms:Phosphinic chloride, dibutyl-;683-16-9;Chlorodibutylphosphine oxide;di-n-butylphosphoryl chloride;SCHEMBL3077216;DIBUTYLPHOSPHINOYL CHLORIDE;DTXSID60382753;AKOS006277724

Suppliers and Price of Phosphinic chloride, dibutyl-

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 Phosphinic chloride, dibutyl-

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:6
Exact Mass:196.0783799
Heavy Atom Count:11
Complexity:124

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCP(=O)(CCCC)Cl

Technology Process of Phosphinic chloride, dibutyl-

There total 3 articles about Phosphinic chloride, dibutyl- 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: 10.0%

: 56-23-5
tetrachloromethane

: 15754-54-8
dibutylphosphine oxide

: 683-16-9
dibutylphosphinic chloride

Guidance literature:: In benzene; at 20 ℃; for 24h;

Reference yield:

: 15754-54-8
dibutylphosphine oxide

: 683-16-9
dibutylphosphinic chloride

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / benzene

2: SOCl₂

With thionyl chloride; triethylamine; In benzene;
DOI:10.1016/S0022-328X(00)86056-8