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1,4-Bis(3-bromopropyl)benzene

Base Information Edit
  • Chemical Name:1,4-Bis(3-bromopropyl)benzene
  • CAS No.:19417-59-5
  • Molecular Formula:C12H16Br2
  • Molecular Weight:320.067
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90544564
  • Wikidata:Q82421707
  • Mol file:19417-59-5.mol
1,4-Bis(3-bromopropyl)benzene

Synonyms:19417-59-5;1,4-Bis-(3-bromopropyl)-benzene;1,4-bis(3-bromopropyl)benzene;Benzene, 1,4-bis(3-bromopropyl)-;SCHEMBL9671990;DTXSID90544564;JMDJLONNYRBOTA-UHFFFAOYSA-N;MFCD14705058;BS-44854;CS-0161842;F16834

Suppliers and Price of 1,4-Bis(3-bromopropyl)benzene
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
Total 18 raw suppliers
Chemical Property of 1,4-Bis(3-bromopropyl)benzene Edit
Chemical Property:
  • Boiling Point:327.2 °C at 760 mmHg 
  • Flash Point:175.7 °C 
  • Density:1.492 g/cm3 
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:6
  • Exact Mass:319.95983
  • Heavy Atom Count:14
  • Complexity:112
Purity/Quality:

99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1CCCBr)CCCBr
  • Use Description Benzene, 1,4-bis(3-bromopropyl)-, is a chemical compound with applications in various fields. In the realm of organic synthesis and the chemical industry, it serves as a valuable intermediate for the production of complex organic molecules. Its bromopropyl groups can be used as reactive functional groups in chemical reactions, enabling the synthesis of polymers, pharmaceuticals, and specialty chemicals. Additionally, in the field of material science, it can be employed as a crosslinking agent in the production of polymers, enhancing their strength and durability. Furthermore, in the field of research, it can be used as a starting material for the development of new compounds and materials with tailored properties. Its adaptability as an intermediate compound underscores its significance in advancing organic synthesis, materials science, and chemical research in various fields.
Technology Process of 1,4-Bis(3-bromopropyl)benzene

There total 11 articles about 1,4-Bis(3-bromopropyl)benzene 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 hydrogen bromide; at 100 ℃; for 2h;
DOI:10.1002/ejoc.200300310
Guidance literature:
Multi-step reaction with 4 steps
1: 67 percent / NaH / benzene / 72 h / 60 °C
2: 91 percent / NiCl2*6H2O; NaBH4 / ethanol / 6 h / 20 °C
3: 81 percent / LiAlH4 / tetrahydrofuran / 3.5 h / 20 °C
4: 81 percent / aq. HBr / 2 h / 100 °C
With sodium tetrahydroborate; lithium aluminium tetrahydride; hydrogen bromide; sodium hydride; nickel dichloride; In tetrahydrofuran; ethanol; benzene; 1: Horner-Emmons reaction;
DOI:10.1002/ejoc.200300310
Guidance literature:
Multi-step reaction with 4 steps
1: Raney Ni, aq. KOH
2: 1) SOCl2, 2) NEt3
3: B2H6
4: HBr
With potassium hydroxide; thionyl chloride; hydrogen bromide; nickel; triethylamine; diborane;
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