(2-Bromo-4,5-dimethoxyphenyl)-phenylmethanone

Base Information

• Chemical Name: (2-Bromo-4,5-dimethoxyphenyl)-phenylmethanone
• CAS No.: 59142-61-9
• Molecular Formula: C15H13BrO3
• Molecular Weight: 321.17
• ChEMBL ID: CHEMBL1171357
• DSSTox Substance ID: DTXSID60488269
• Wikidata: Q82330832

Synonyms:(2-bromo-4,5-dimethoxyphenyl)-phenylmethanone;59142-61-9;CHEMBL1171357;SCHEMBL11008513;DTXSID60488269;QCMQYFUIIQLFJC-UHFFFAOYSA-N;(2-bromo-4,5-dimethoxyphenyl)phenylmethanone;(2-Bromo-4,5-dimethoxyphenyl)(phenyl)methanone

Chemical Property of (2-Bromo-4,5-dimethoxyphenyl)-phenylmethanone

Chemical Property:

• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 320.00481
• Heavy Atom Count: 19
• Complexity: 302

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=C(C(=C1)C(=O)C2=CC=CC=C2)Br)OC

Technology Process of (2-Bromo-4,5-dimethoxyphenyl)-phenylmethanone

There total 8 articles about (2-Bromo-4,5-dimethoxyphenyl)-phenylmethanone 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: 97.0%

(2-bromo-4,5-dimethoxyphenyl)phenylmethanol (59142-62-0) → 2-benzoyl-4, 5-dimethoxyl-1-bromobenzene (59142-61-9)

Guidance literature:

With silica gel; pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;

DOI:10.1021/jo402763m

Reference yield: 91.0%

3,4-dimethoxybenzophenone (4038-14-6) → 2-benzoyl-4, 5-dimethoxyl-1-bromobenzene (59142-61-9)

Guidance literature:

With bromine; acetic acid; at 20 ℃; for 4h; regioselective reaction;

DOI:10.1016/j.bmcl.2010.05.068

Reference yield:

4-Bromoveratrole (2859-78-1) → 2-benzoyl-4, 5-dimethoxyl-1-bromobenzene (59142-61-9)

Guidance literature:

With benzoic acid;

upstream raw materials:

(2-bromo-4,5-dimethoxyphenyl)phenylmethanol

4-Bromoveratrole

3,4-dimethoxybenzophenone

benzene

Downstream raw materials:

2,3-Dimethoxyfluoren-9-one

(2-bromo-4,5-dimethoxyphenyl)phenylmethane

(2-bromo-4,5-dimethoxyphenyl)(diphenyl)methanol

1-(2-bromo-4,5-dimethoxyphenyl)-1-phenylethanol

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