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7-Bromomethylfluoranthene

Base Information
  • Chemical Name:7-Bromomethylfluoranthene
  • CAS No.:77061-07-5
  • Molecular Formula:C17H11Br
  • Molecular Weight:295.178
  • Hs Code.:2903999090
  • UNII:VCK2CJ2GZ5
  • DSSTox Substance ID:DTXSID20227858
  • Wikidata:Q83107696
  • Mol file:77061-07-5.mol
7-Bromomethylfluoranthene

Synonyms:7-Bromomethylfluoranthene;77061-07-5;VCK2CJ2GZ5;7-(bromomethyl)fluoranthene;CCRIS 5206;UNII-VCK2CJ2GZ5;SCHEMBL16201010;DTXSID20227858;FLUORANTHENE, 7-(BROMOMETHYL)-

Suppliers and Price of 7-Bromomethylfluoranthene
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
  • American Custom Chemicals Corporation
  • 7-BROMOMETHYLFLUORANTHENE 95.00%
  • 5MG
  • $ 503.01
Total 1 raw suppliers
Chemical Property of 7-Bromomethylfluoranthene
Chemical Property:
  • Vapor Pressure:1.22E-07mmHg at 25°C 
  • Melting Point:105-107 °C 
  • Boiling Point:443.3°C at 760 mmHg 
  • Flash Point:225.5°C 
  • PSA:0.00000 
  • Density:1.541g/cm3 
  • LogP:5.38210 
  • XLogP3:5.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:1
  • Exact Mass:294.00441
  • Heavy Atom Count:18
  • Complexity:313
Purity/Quality:

7-BROMOMETHYLFLUORANTHENE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=C3C(=C1)C4=CC=CC(=C4C3=CC=C2)CBr
Technology Process of 7-Bromomethylfluoranthene

There total 2 articles about 7-Bromomethylfluoranthene 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; Perbenzoic acid; In tetrachloromethane; for 3h; Heating;
DOI:10.1021/jo00325a028
Guidance literature:
Multi-step reaction with 2 steps
1: 80 percent / DDQ / xylene / 5 h / Heating
2: 80 percent / N-bromosuccinimide, benzoyl peroxide / CCl4 / 3 h / Heating
With N-Bromosuccinimide; Perbenzoic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrachloromethane; xylene;
DOI:10.1021/jo00325a028
Guidance literature:
Multi-step reaction with 10 steps
1: 78 percent / diethyl ether / 30 h / Heating
2: 1.) diborane, 2.) 30percent H2O2 / 1.) THF, from 0 deg C to room temp., 8 h, 2.) reflux, 1 h
3: pyridinium chlorochromate / CH2Cl2 / 1 h / 20 °C
4: 85 percent / AgNO3, 1.5 KOH / ethanol; H2O / 2 h
5: SOCl2 / benzene / 3 h / Heating
6: 1.) AlCl3 / CS2 / 1.) 0 deg C, 2.) reflux, 10 min
7: LiAlH4 / tetrahydrofuran / 0.33 h / 20 °C
8: 60 percent / conc. H2SO4 / acetic acid / 3 h / 60 °C
9: 62 percent / 1.) I2 / benzene / 1.) reflux, 2.) reflux, 2.5 h
10: 30 percent / N-bromsuccinimide, α,α'-azobis(isobutyronitrile) / CCl4 / 2 h / Heating
With potassium hydroxide; N-Bromosuccinimide; lithium aluminium tetrahydride; aluminium trichloride; thionyl chloride; sulfuric acid; azobisisobutyronitrile; dihydrogen peroxide; iodine; silver nitrate; pyridinium chlorochromate; diborane; In tetrahydrofuran; carbon disulfide; tetrachloromethane; diethyl ether; ethanol; dichloromethane; water; acetic acid; benzene;
DOI:10.1021/jo00325a028
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