Dichloro-(ethoxy)borane

Base Information

Chemical Name:Dichloro-(ethoxy)borane
CAS No.:16339-28-9
Molecular Formula:C2H5 B Cl2 O
Molecular Weight:126.778
Hs Code.:2931900090
DSSTox Substance ID:DTXSID30167579
Wikidata:Q83036978
Mol file:16339-28-9.mol

Synonyms:Dichloro-(ethoxy)borane;dichloro(ethoxy)borane;16339-28-9;Borane, dichloroethoxy-;SCHEMBL4300921;CEUSKTVXHGPJDP-UHFFFAOYSA-;DTXSID30167579

Suppliers and Price of Dichloro-(ethoxy)borane

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 Dichloro-(ethoxy)borane

Chemical Property:

Vapor Pressure:102mmHg at 25°C
Boiling Point:78.7°Cat760mmHg
Flash Point:1.4°C
PSA：9.23000
Density:1.125g/cm³
LogP:1.48540
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:125.9810503
Heavy Atom Count:6
Complexity:32.7

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:B(OCC)(Cl)Cl

Technology Process of Dichloro-(ethoxy)borane

There total 5 articles about Dichloro-(ethoxy)borane 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: 80.0%

: 98815-02-2
6,6,6-tris(dimethylphenylphosphine)-6-hydrido-6-Re-nido-B₉H₁₂-9-OEt

: 116085-79-1
2,2,2-tris(dimethylphenylphosphine)-2,2-dihydrido-2-rhena-nido-nonaborane

: 15075-90-8
C₂⁽²⁾H₂Cl₂

: 16339-28-9
ethoxy-dichloroborane

Guidance literature:: In further solvent(s); thermolysis in sym C2D2Cl4 at 100°C under N2 for 45 min; evapd., isolated by repeated preparative t.l.c. (silica gel, CH2Cl2, then Et2O/pentane 1/4);