Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Borane, chlorodiphenyl-

Base Information Edit
  • Chemical Name:Borane, chlorodiphenyl-
  • CAS No.:3677-81-4
  • Molecular Formula:C12H10BCl
  • Molecular Weight:200.475
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10415984
  • Nikkaji Number:J673.531B
  • Wikidata:Q82225087
  • Mol file:3677-81-4.mol
Borane, chlorodiphenyl-

Synonyms:Borane, chlorodiphenyl-;diphenylchloroborane;3677-81-4;chloro(diphenyl)borane;chlorodiphenylborane;SCHEMBL2218862;DTXSID10415984;InChI=1/C12H10BCl/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10

Suppliers and Price of Borane, chlorodiphenyl-
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 34 raw suppliers
Chemical Property of Borane, chlorodiphenyl- Edit
Chemical Property:
  • PSA:0.00000 
  • LogP:2.03110 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:2
  • Exact Mass:200.0564082
  • Heavy Atom Count:14
  • Complexity:142
Purity/Quality:

99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:B(C1=CC=CC=C1)(C2=CC=CC=C2)Cl
Technology Process of Borane, chlorodiphenyl-

There total 34 articles about Borane, chlorodiphenyl- 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:
Guidance literature:
distn. of BCl3 into (C6H5)2BN(C2H5)2 at -50°C; distn.;
DOI:10.1016/0022-328X(68)80063-4
Guidance literature:
With octene-1; Bis(borolane); In xylene; introduction of BCl3 into soln. of B(C6H5)3 and bis(borolane), stirring at 120°C for 15 min (cooler at -78°C), addn. of octene-1; vac. distn; further product obtained by adding bis(borolane) to unified residue and predistillate and repeating procedure;
Guidance literature:
In benzene; pouring BCl3 in soln. of Sn(C6H5)4 at 10°C, boiling under reflux (cooler at -78°C) for 3 h, with water temp. cooler for further 48 h; removing benzene by distn., twofold fractionated distn. of product at reduced pressure;
Post RFQ for Price