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Naphtho[2,3-B]benzofuran-1-ylboronic acid

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Naphtho[2,3-B]benzofuran-1-ylboronic acid Basic information

Product Name:
Naphtho[2,3-B]benzofuran-1-ylboronic acid
Synonyms:
  • Naphtho[2,3-b]benzofuran-1-ylboronic acid
  • Benzo[b]naphtho[2,3-d]furan-1-yl-boronic acid
  • Naphthalene [2, 3-b] benzofuran-1-boric acid
CAS:
2261008-21-1
MF:
C16H11BO3
MW:
262.07
Mol File:
2261008-21-1.mol
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Naphtho[2,3-B]benzofuran-1-ylboronic acid Chemical Properties

Boiling point:
529.2±42.0 °C(Predicted)
Density 
1.37±0.1 g/cm3(Predicted)
pka
8.20±0.30(Predicted)
InChI
InChI=1S/C16H11BO3/c18-17(19)13-6-3-7-14-16(13)12-8-10-4-1-2-5-11(10)9-15(12)20-14/h1-9,18-19H
InChIKey
GUPYETLVSSDKRR-UHFFFAOYSA-N
SMILES
B(C1=C2C3=CC4C(=CC=CC=4)C=C3OC2=CC=C1)(O)O
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Naphtho[2,3-B]benzofuran-1-ylboronic acid Usage And Synthesis

Chemical Properties

Naphtho[2,3-B]benzofuran-1-ylboronic acid is a red-brown crystalline powder.
It is very soluble in N,N-Dimethylformamide,Soluble in methanol,Sparingly soluble inglacial acetic acid, Very slightly soluble inchloroform, Practically insoluble in water.

Uses

Naphtho[2,3-B]benzofuran-1-ylboronic acid is a chemical compound with the formula C16H11BO3 and a molecular weight of 262.07g/mol. It is mainly used to make liquid crystals.

Application

Naphtho[2,3-B]benzofuran-1-ylboronic acid could used to synthesize organic compound which could used as the host material of the light-emitting layer organic electroluminescence element.

Preparation

Naphtho[2,3-b]benzofuran-2-ylboronic acid can be synthesized using several methods, including Suzuki-Miyaura cross-coupling reactions, boronate esterification, and direct boronic acid functionalization.

Biological Activity

Naphtho[2,3-b]benzofuran-2-ylboronic acid has been found to exert various effects on cell function and signal transduction. It can influence cellular processes, including proliferation, apoptosis, and differentiation. Additionally, this compound has demonstrated potential therapeutic effects in the treatment of certain diseases, such as cancer, neurodegenerative disorders, and inflammatory conditions.

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