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Benzene-1,3,5-triyltriboronic acid

Base Information
  • Chemical Name:Benzene-1,3,5-triyltriboronic acid
  • CAS No.:89641-21-4
  • Molecular Formula:C6H9B3O6
  • Molecular Weight:209.567
  • Hs Code.:
  • European Community (EC) Number:865-208-3
  • Nikkaji Number:J1.171.854J
Benzene-1,3,5-triyltriboronic acid

Synonyms:BENZENE-1,3,5-TRIYLTRIBORONIC ACID;89641-21-4;Boronic acid, 1,3,5-benzenetriyltris-;(3,5-diboronophenyl)boronic acid;YSZC207;SCHEMBL806837;AMY027;benzene-1,3,5-triboronic acid;MFCD20275289;AKOS030627453;AS-47075;BENZENE-1,3,5-TRIYLTRIBORONICACID;DB-369813;CS-0111293;F11883;3,5-BIS(DIHYDROXYBORANYL)PHENYLBORONIC ACID

Suppliers and Price of Benzene-1,3,5-triyltriboronic 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
Total 20 raw suppliers
Chemical Property of Benzene-1,3,5-triyltriboronic acid
Chemical Property:
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:210.0678285
  • Heavy Atom Count:15
  • Complexity:156
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:B(C1=CC(=CC(=C1)B(O)O)B(O)O)(O)O
Technology Process of Benzene-1,3,5-triyltriboronic acid

There total 4 articles about Benzene-1,3,5-triyltriboronic 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:
1,3,5-tris(trimethylsilyl)benzene; boron tribromide; at 100 ℃; for 4h; Inert atmosphere;
water; In hexane; at 0 ℃;
Guidance literature:
1,3,5-tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene; With sodium periodate; In tetrahydrofuran; water; at 20 ℃;
With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃; for 24h;
DOI:10.1002/anie.201308924
Guidance literature:
Multi-step reaction with 2 steps
1.1: potassium acetate; bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / 120 °C / Inert atmosphere; Schlenk technique
2.1: sodium periodate / tetrahydrofuran; water / 20 °C / Inert atmosphere; Schlenk technique
2.2: Inert atmosphere; Schlenk technique
With bis-triphenylphosphine-palladium(II) chloride; sodium periodate; potassium acetate; In tetrahydrofuran; 1,4-dioxane; water;
DOI:10.1039/c8cc04870c
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