(2-Bromo-4-methoxyphenyl)(2,5-dimethylphenyl)methanone

Base Information

Chemical Name:(2-Bromo-4-methoxyphenyl)(2,5-dimethylphenyl)methanone
CAS No.:89651-82-1
Molecular Formula:C₁₆H₁₅BrO₂
Molecular Weight:319.198
Hs Code.:
DSSTox Substance ID:DTXSID00529509
Wikidata:Q82399966

Synonyms:89651-82-1;(2-Bromo-4-methoxyphenyl)(2,5-dimethylphenyl)methanone;DTXSID00529509;AKOS005912415

Suppliers and Price of (2-Bromo-4-methoxyphenyl)(2,5-dimethylphenyl)methanone

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 (2-Bromo-4-methoxyphenyl)(2,5-dimethylphenyl)methanone

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:318.02554
Heavy Atom Count:19
Complexity:318

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C=C1)C)C(=O)C2=C(C=C(C=C2)OC)Br

Technology Process of (2-Bromo-4-methoxyphenyl)(2,5-dimethylphenyl)methanone

There total 1 articles about (2-Bromo-4-methoxyphenyl)(2,5-dimethylphenyl)methanone 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: 0.9%

: 2398-37-0
3-methoxyphenyl bromide

: 610-72-0
2,5-dimethylbenzoic acid

: 89651-82-1
2-bromo-4-methoxy-2',5'-dimethylbenzophenone

: 2-bromo-6-methoxy-2',5'-dimethyl-benzophenone

Guidance literature:: With 1H-imidazole; trifluoroacetic anhydride; In trifluoroacetic acid; for 20h; Heating;
DOI:10.1016/S0040-4020(01)88629-4