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4-diphenyl-1-naphthalene boronic acid

Base Information
  • Chemical Name:4-diphenyl-1-naphthalene boronic acid
  • CAS No.:881811-83-2
  • Molecular Formula:C22H17BO2
  • Molecular Weight:324.18000
  • Hs Code.:2931900090
4-diphenyl-1-naphthalene boronic acid

Synonyms:4-diphenyl-1-naphthalene boronic acid;

Suppliers and Price of 4-diphenyl-1-naphthalene boronic acid
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-Diphenyl-1-naphthaleneboronicacid 97%
  • 1g
  • $ 258.00
  • Crysdot
  • 4-Diphenyl-1-naphthaleneboronicacid 97%
  • 5g
  • $ 773.00
  • American Custom Chemicals Corporation
  • 4-DIPHENYL-1-NAPHTHALENE BORONIC ACID 95.00%
  • 5MG
  • $ 504.24
  • Alichem
  • 4-Diphenyl-1-naphthaleneboronicacid
  • 5g
  • $ 811.65
Total 32 raw suppliers
Chemical Property of 4-diphenyl-1-naphthalene boronic acid
Chemical Property:
  • Boiling Point:528.1±60.0 °C(Predicted) 
  • PKA:8.56±0.30(Predicted) 
  • PSA:40.46000 
  • Density:1.24±0.1 g/cm3(Predicted) 
  • LogP:3.85360 
Purity/Quality:

99% *data from raw suppliers

4-Diphenyl-1-naphthaleneboronicacid 97% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4-diphenyl-1-naphthalene boronic acid

There total 5 articles about 4-diphenyl-1-naphthalene boronic acid 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 hydrogenchloride; In tetrahydrofuran; hexane;
DOI:10.1021/ja058066n
Guidance literature:
Multi-step reaction with 3 steps
1.1: aq. H2SO4 / 8 h / 50 °C
1.2: aq. NaNO2 / 0.5 h / 0 °C
1.3: 79 percent / aq. KI / 4 h / Heating
2.1: n-BuLi / hexane; tetrahydrofuran / 0.5 h / -78 °C
2.2: hexane; tetrahydrofuran / 20 °C
3.1: 147 mg / aq. HCl / hexane; tetrahydrofuran
With hydrogenchloride; n-butyllithium; sulfuric acid; In tetrahydrofuran; hexane;
DOI:10.1021/ja058066n
Guidance literature:
Multi-step reaction with 4 steps
1.1: 68 percent / Pd(OAc)2; PPh3; Cs2CO3 / dimethylformamide / 12 h / 90 °C
2.1: aq. H2SO4 / 8 h / 50 °C
2.2: aq. NaNO2 / 0.5 h / 0 °C
2.3: 79 percent / aq. KI / 4 h / Heating
3.1: n-BuLi / hexane; tetrahydrofuran / 0.5 h / -78 °C
3.2: hexane; tetrahydrofuran / 20 °C
4.1: 147 mg / aq. HCl / hexane; tetrahydrofuran
With hydrogenchloride; palladium diacetate; n-butyllithium; sulfuric acid; caesium carbonate; triphenylphosphine; In tetrahydrofuran; hexane; N,N-dimethyl-formamide; 1.1: Suzuki-Miyaura coupling;
DOI:10.1021/ja058066n
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