(1,2-Dimethyl-2-phenylcyclopropyl)benzene

Base Information

Chemical Name:(1,2-Dimethyl-2-phenylcyclopropyl)benzene
CAS No.:32134-42-2
Molecular Formula:C17H18
Molecular Weight:222.32500
Hs Code.:
DSSTox Substance ID:DTXSID40394738
Mol file:32134-42-2.mol

Synonyms:(1,2-dimethyl-2-phenylcyclopropyl)benzene;32134-42-2;DTXSID40394738;AE-562/12222013

Suppliers and Price of (1,2-Dimethyl-2-phenylcyclopropyl)benzene

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 0 raw suppliers

Chemical Property of (1,2-Dimethyl-2-phenylcyclopropyl)benzene

Chemical Property:

PSA：0.00000
LogP:4.30590
XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:2
Exact Mass:222.140850574
Heavy Atom Count:17
Complexity:242

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(CC1(C)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of (1,2-Dimethyl-2-phenylcyclopropyl)benzene

There total 6 articles about (1,2-Dimethyl-2-phenylcyclopropyl)benzene 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%

: 54398-02-6,61894-39-1,342043-00-9
1,1-Dichlor-r-2,t-3-dimethyl-2,c-3-diphenylcyclopropan

: 32134-42-2
C₁₇H₁₈

Guidance literature:: With sodium; tert-butyl alcohol; In tetrahydrofuran; for 12h; Heating;
DOI:10.1002/jps.2600711012

Reference yield:

: 782-06-9
(E)-2,3-diphenylbutene

: 32134-42-2
C₁₇H₁₈

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / aq. sodium hydroxide, triethylbenzylammonium chloride

2: 80 percent / sodium, tert-butyl alcohol / tetrahydrofuran / 12 h / Heating

With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; sodium; tert-butyl alcohol; In tetrahydrofuran;
DOI:10.1002/jps.2600711012