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3-(Bromomethyl)phenyl benzoate

Base Information Edit
  • Chemical Name:3-(Bromomethyl)phenyl benzoate
  • CAS No.:129250-89-1
  • Molecular Formula:C14H11BrO2
  • Molecular Weight:291.144
  • Hs Code.:
  • European Community (EC) Number:673-921-4
  • DSSTox Substance ID:DTXSID40366011
  • Wikidata:Q82151058
  • Mol file:129250-89-1.mol
3-(Bromomethyl)phenyl benzoate

Synonyms:3-(bromomethyl)phenyl benzoate;[3-(bromomethyl)phenyl] benzoate;129250-89-1;benzoic acid 3-bromomethylphenyl ester;SCHEMBL4216005;DTXSID40366011;VJGOZOYBJUTQKK-UHFFFAOYSA-N;STL115515;AKOS003591050

Suppliers and Price of 3-(Bromomethyl)phenyl benzoate
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • BENZOIC ACID-3-BROMOMETHYLPHENYL ESTER 98.00%
  • 5G
  • $ 1530.38
  • AHH
  • Benzoicacid3-bromomethylphenylester 98%
  • 5g
  • $ 470.00
Total 5 raw suppliers
Chemical Property of 3-(Bromomethyl)phenyl benzoate Edit
Chemical Property:
  • PSA:26.30000 
  • LogP:3.80070 
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:289.99424
  • Heavy Atom Count:17
  • Complexity:249
Purity/Quality:

98%min *data from raw suppliers

BENZOIC ACID-3-BROMOMETHYLPHENYL ESTER 98.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=O)OC2=CC=CC(=C2)CBr
Technology Process of 3-(Bromomethyl)phenyl benzoate

There total 3 articles about 3-(Bromomethyl)phenyl benzoate 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:
Guidance literature:
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; for 0.5h; Heating;
DOI:10.1021/jm001028o
Guidance literature:
Multi-step reaction with 2 steps
1: 42 percent / 2 N NaOH / 0.25 h / 0 °C
2: 60 percent / N-bromosuccinimide; N,N'-azobis(isobutyronitrile) / CCl4 / 0.5 h / Heating
With sodium hydroxide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane;
DOI:10.1021/jm001028o
Guidance literature:
Multi-step reaction with 2 steps
1: 42 percent / 2 N NaOH / 0.25 h / 0 °C
2: 60 percent / N-bromosuccinimide; N,N'-azobis(isobutyronitrile) / CCl4 / 0.5 h / Heating
With sodium hydroxide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane;
DOI:10.1021/jm001028o
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