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4-(BroMoMethyl)-2-naphthonitrile

Base Information
  • Chemical Name:4-(BroMoMethyl)-2-naphthonitrile
  • CAS No.:79997-04-9
  • Molecular Formula:C12H8BrN
  • Molecular Weight:246.10262
  • Hs Code.:
  • Mol file:79997-04-9.mol
4-(BroMoMethyl)-2-naphthonitrile

Synonyms:4-(BroMoMethyl)-2-naphthonitrile

Suppliers and Price of 4-(BroMoMethyl)-2-naphthonitrile
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
  • Crysdot
  • 4-(Bromomethyl)-2-naphthonitrile 95+%
  • 1g
  • $ 853.00
  • Chemenu
  • 4-(bromomethyl)-2-naphthonitrile 95%
  • 1g
  • $ 805.00
  • Alichem
  • 1-(Bromomethyl)-3-cyanonaphthalene
  • 1g
  • $ 1735.55
  • Alichem
  • 1-(Bromomethyl)-3-cyanonaphthalene
  • 500mg
  • $ 1009.40
  • Alichem
  • 1-(Bromomethyl)-3-cyanonaphthalene
  • 250mg
  • $ 680.00
Total 4 raw suppliers
Chemical Property of 4-(BroMoMethyl)-2-naphthonitrile
Chemical Property:
  • PSA:23.79000 
  • LogP:3.60638 
  • Storage Temp.:2-8°C 
Purity/Quality:

≥99% *data from raw suppliers

4-(Bromomethyl)-2-naphthonitrile 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4-(BroMoMethyl)-2-naphthonitrile

There total 4 articles about 4-(BroMoMethyl)-2-naphthonitrile 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 pyridine; phosphorus tribromide; In benzene; at 55 ℃; for 6h;
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) yellow mercuric oxide; 2.) hydchloric acid / 1.) aq. acetic acid; 2.) water
2: 100 percent / LiAlH4 / diethyl ether / 1.) reflux, 3 h; 2.) room temperature, 14 h
3: 51 percent
4: 90 percent / PBr3, pyridine / benzene / 6 h / 55 °C
With pyridine; hydrogenchloride; lithium aluminium tetrahydride; phosphorus tribromide; mercury(II) oxide; In diethyl ether; benzene;
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / LiAlH4 / diethyl ether / 1.) reflux, 3 h; 2.) room temperature, 14 h
2: 51 percent
3: 90 percent / PBr3, pyridine / benzene / 6 h / 55 °C
With pyridine; lithium aluminium tetrahydride; phosphorus tribromide; In diethyl ether; benzene;
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