(1,1'-Biphenyl)-2-ol, phosphite (3:1)

Base Information Edit

Chemical Name:(1,1'-Biphenyl)-2-ol, phosphite (3:1)
CAS No.:2752-19-4
Molecular Formula:C36H27 O3 P
Molecular Weight:538.582
Hs Code.:2919900090
European Community (EC) Number:220-396-0
DSSTox Substance ID:DTXSID20950199
Nikkaji Number:J39.606K
Wikidata:Q82928198
Mol file:2752-19-4.mol

Synonyms:2752-19-4;tris(2-phenylphenyl) phosphite;(1,1'-Biphenyl)-2-ol, phosphite (3:1);[1,1'-Biphenyl]-2-ol, phosphite (3:1);EINECS 220-396-0;TRIS ORTHO XENYL PHOSPHITE, 95;(1,1'-Biphenyl)-2-ol, 2,2'',2''''-phosphite;Tris((1,1'-biphenyl)-2-oxy)phosphine;Tris[[1,1'-biphenyl]-2-oxy]phosphine;tris(2-phenylphenyl)phosphite;SCHEMBL674709;tri-(o-bi-phenylyl) phosphite;tris(o-phenylphenyl) phosphite;Tris(biphenyl-2-yl)-phosphite;tris(orthophenylphenyl)phosphite;C36H27O3P;DTXSID20950199;C36-H27-O3-P;Tri[1,1'-biphenyl]-2-yl phosphite;2-([Bis([1,1'-biphenyl]-2-yloxy)phosphino]oxy)-1,1'-biphenyl #

Suppliers and Price of (1,1'-Biphenyl)-2-ol, phosphite (3:1)

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 8 raw suppliers

Chemical Property of (1,1'-Biphenyl)-2-ol, phosphite (3:1) Edit

Chemical Property:

Melting Point:93°C
Boiling Point:654°Cat760mmHg
Flash Point:440.7°C
PSA：41.28000
Density:g/cm³
LogP:10.45130
XLogP3:10.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:9
Exact Mass:538.16978172
Heavy Atom Count:40
Complexity:618

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC=CC=C2OP(OC3=CC=CC=C3C4=CC=CC=C4)OC5=CC=CC=C5C6=CC=CC=C6

Technology Process of (1,1'-Biphenyl)-2-ol, phosphite (3:1)

There total 4 articles about (1,1'-Biphenyl)-2-ol, phosphite (3:1) 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: 42.5%