1,5-Diphenylbicyclo[3.2.0]heptane

Base Information

Chemical Name:1,5-Diphenylbicyclo[3.2.0]heptane
CAS No.:94383-67-2
Molecular Formula:C₁₉H₂₀
Molecular Weight:248.368
Hs Code.:2902909090
DSSTox Substance ID:DTXSID50915579
Mol file:94383-67-2.mol

Synonyms:1,5-Diphenylbicyclo[3.2.0]heptane;94383-67-2;1,5-Diphenylbicyclo(3.2.0)heptane;DTXSID50915579;ITJCELKBMFHZCC-UHFFFAOYSA-N

Suppliers and Price of 1,5-Diphenylbicyclo[3.2.0]heptane

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 4 raw suppliers

Chemical Property of 1,5-Diphenylbicyclo[3.2.0]heptane

Chemical Property:

Vapor Pressure:0.000108mmHg at 25°C
Boiling Point:347.4°Cat760mmHg
Flash Point:174.7°C
PSA：0.00000
Density:1.113g/cm³
LogP:4.84010
XLogP3:6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:2
Exact Mass:248.156500638
Heavy Atom Count:19
Complexity:289

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2(CCC2(C1)C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of 1,5-Diphenylbicyclo[3.2.0]heptane

There total 10 articles about 1,5-Diphenylbicyclo[3.2.0]heptane 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: 98.0%

: 27905-65-3
2,6-Diphenyl-1,6-heptadiene

: 94383-67-2,125024-90-0
1,5-Diphenylbicyclo<3.2.0>heptane

Guidance literature:: With 7,8-dimethoxy-3-methylalloxazine immobilized on mesoporous silica; In acetonitrile; for 2h; diastereoselective reaction; Schlenk technique; Inert atmosphere; Irradiation;
DOI:10.1002/cctc.201601654