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6-Benzyloxy-2-naphthylboronic acid

Base Information
  • Chemical Name:6-Benzyloxy-2-naphthylboronic acid
  • CAS No.:152915-83-8
  • Molecular Formula:C17H15BO3
  • Molecular Weight:278.11
  • Hs Code.:2931900090
  • DSSTox Substance ID:DTXSID90383273
  • Wikidata:Q82174941
  • Mol file:152915-83-8.mol
6-Benzyloxy-2-naphthylboronic acid

Synonyms:152915-83-8;6-Benzyloxy-2-naphthylboronic acid;6-(Benzyloxy)-2-naphthylboronic acid;6-Benzyloxynaphthalene-2-boronic acid;6-(benzyloxy)naphthalen-2-ylboronic acid;(6-phenylmethoxynaphthalen-2-yl)boronic Acid;Boronic acid,B-[6-(phenylmethoxy)-2-naphthalenyl]-;[6-(benzyloxy)naphthalen-2-yl]boronic acid;(6-(Benzyloxy)naphthalen-2-yl)boronic acid;SCHEMBL257567;DTXSID90383273;6-Benzyloxy-2-naphthylboronicacid;CGA91583;MFCD04115402;AKOS004119294;AB19956;BS-27515;CS-0174971;FT-0715065;D71319;A883864

Suppliers and Price of 6-Benzyloxy-2-naphthylboronic 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
  • TRC
  • 6-Benzyloxynaphthalene-2-boronicAcid
  • 1g
  • $ 75.00
  • TRC
  • 6-Benzyloxynaphthalene-2-boronicAcid
  • 100mg
  • $ 45.00
  • Matrix Scientific
  • 6-Benzyloxy-2-naphthylboronic acid 95+%
  • 5g
  • $ 908.00
  • AOBChem
  • 6-(Benzyloxy)-2-naphthylboronicacid 97%
  • 100g
  • $ 1608.00
  • American Custom Chemicals Corporation
  • 6-(BENZYLOXY)-2-NAPHTHYLBORONIC ACID 95.00%
  • 1G
  • $ 374.85
  • American Custom Chemicals Corporation
  • 6-(BENZYLOXY)-2-NAPHTHYLBORONIC ACID 95.00%
  • 5G
  • $ 1517.16
  • Alichem
  • 6-Benzyloxy-2-naphthylboronicacid
  • 25g
  • $ 998.00
  • AK Scientific
  • 6-Benzyloxynaphthalene-2-boronicacid
  • 5g
  • $ 291.00
Total 23 raw suppliers
Chemical Property of 6-Benzyloxy-2-naphthylboronic acid
Chemical Property:
  • Vapor Pressure:3.06E-11mmHg at 25°C 
  • Refractive Index:1.655 
  • Boiling Point:510.4 °C at 760 mmHg 
  • Flash Point:262.5 °C 
  • PSA:49.69000 
  • Density:1.24 g/cm3 
  • LogP:2.09860 
  • Storage Temp.:Room temperature. 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:278.1114245
  • Heavy Atom Count:21
  • Complexity:317
Purity/Quality:

97% *data from raw suppliers

6-Benzyloxynaphthalene-2-boronicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s): R36/37/38:Irritating to eyes, respiratory system and skin.; 
  • Hazard Codes: Xi:Irritant;
     
  • Statements: R36/37/38:Irritating to eyes, respiratory system and skin.; 
  • Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S37/39:Wear suitable g 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:B(C1=CC2=C(C=C1)C=C(C=C2)OCC3=CC=CC=C3)(O)O
Technology Process of 6-Benzyloxy-2-naphthylboronic acid

There total 6 articles about 6-Benzyloxy-2-naphthylboronic 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;
DOI:10.1016/j.bmcl.2006.08.025
Guidance literature:
6-benzyloxy-2-bromonaphthalene; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.166667h;
Triisopropyl borate; In tetrahydrofuran; at -78 ℃; for 1.75h;
With hydrogenchloride; In tetrahydrofuran; water;
DOI:10.1002/chem.201403630
Guidance literature:
Multi-step reaction with 3 steps
1.1: NaH / dimethylformamide / 1 h / 0 - 20 °C
2.1: BuLi / tetrahydrofuran / -78 °C
2.2: tetrahydrofuran / 16 h / 20 °C
3.1: 81 percent / HCl
With hydrogenchloride; n-butyllithium; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2006.08.025
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