Benzene, 2-methoxy-1-methyl-3-(2-phenylethenyl)-, (E)-

Base Information

Chemical Name:Benzene, 2-methoxy-1-methyl-3-(2-phenylethenyl)-, (E)-
CAS No.:122950-68-9
Molecular Formula:C₁₆H₁₆O
Molecular Weight:224.302
Hs Code.:
DSSTox Substance ID:DTXSID001209538

Synonyms:DTXSID001209538;Benzene, 2-methoxy-1-methyl-3-(2-phenylethenyl)-, (E)-;122950-68-9

Suppliers and Price of Benzene, 2-methoxy-1-methyl-3-(2-phenylethenyl)-, (E)-

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
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Total 0 raw suppliers

Chemical Property of Benzene, 2-methoxy-1-methyl-3-(2-phenylethenyl)-, (E)-

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:224.120115130
Heavy Atom Count:17
Complexity:240

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=CC=C1)C=CC2=CC=CC=C2)OC
Isomeric SMILES:CC1=C(C(=CC=C1)/C=C/C2=CC=CC=C2)OC

Technology Process of Benzene, 2-methoxy-1-methyl-3-(2-phenylethenyl)-, (E)-

There total 3 articles about Benzene, 2-methoxy-1-methyl-3-(2-phenylethenyl)-, (E)- 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:

: 1004-66-6
2-methoxy-1,3-dimethylbenzene

: 122950-68-9
trans-2-methoxy-3-methylstilbene

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / N-bromosuccinimide, benzoyl peroxide / CCl₄ / Heating

With N-Bromosuccinimide; Perbenzoic acid; In tetrachloromethane;
DOI:10.1021/jo00280a032