1-Naphthaleneboronic acid

Product Information

Molecular Formula:
C10H9BO2
Molecular Weight:
171.99
Description
1-Naphthaleneboronic acid (CAS# 13922-41-3 ) is a useful research chemical.
Synonyms
1-Naphthylboronic acid; Naphthalene-1-boronic acid
IUPAC Name
naphthalen-1-ylboronic acid
Canonical SMILES
B(C1=CC=CC2=CC=CC=C12)(O)O
InChI
InChI=1S/C10H9BO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7,12-13H
InChI Key
HUMMCEUVDBVXTQ-UHFFFAOYSA-N
Boiling Point
381.9 °C at 760 mmHg
Melting Point
210-211 °C
Flash Point
Not applicable
Purity
95 %
Density
1.21 g/cm3
Appearance
Off-white to pink beige powder
Storage
0-6 °C

Safety Information

Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338
Signal Word
Warning

Computed Properties

Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
1
Exact Mass
172.0695597 g/mol
Monoisotopic Mass
172.0695597 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
172
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114031475-A Bromine simple substance-promoted extremely-low-dose palladium-catalyzed water-phase Suzuki coupling reaction method 2021-12-24
CN-114106056-A Metal organic light-emitting material and application thereof in OLED device 2021-12-02
CN-114163384-A Method for synthesizing polysubstituted 5-acyl nicotinonitrile 2021-12-01
CN-114106050-A Tight chiral environment biphenyl-phenanthrene framework chiral phosphoric acid and preparation method and application thereof 2021-11-29
CN-113694968-A Palladium-loaded magnetic UiO-66 ternary composite catalytic material and preparation method and application thereof 2021-09-27
CN-114058045-A Organic room temperature phosphorescent thin film material with hydrothermal stimulus response and excitation dependence, preparation and application 2021-09-13
CN-113620901-A Crown ether derived chiral 1,1 '-bi-2, 2' -naphthol, preparation method and application thereof 2021-08-31
AU-2021105218-A4 Cultivation method of high-quality early-maturing cotton suitable for mechanized production 2021-08-10
CN-113549081-A Organic compound and organic electroluminescent device using same 2021-07-26
CN-113402507-A Triphenylene derivative, light-emitting device material, and light-emitting device 2021-07-10

Literatures

PMID Publication Date Title Journal
22091128 2011-08-01 4,6-Dimethyl-2-(naphthalen-1-yl)pyrimidine Acta crystallographica. Section E, Structure reports online
21582783 2009-06-06 tert-Butyl N-hydr-oxy-N-[(1S*,2R*)-2-(1-naphth-yl)cyclo-pent-3-en-1-yl]carbamate Acta crystallographica. Section E, Structure reports online
21583951 2009-04-30 2-[1-(1-Naphth-yl)-1H-1,2,3-triazol-4-yl]pyridine Acta crystallographica. Section E, Structure reports online
21202048 2008-03-05 4-Amino-13-(1-naphth-yl)-[2,2]paracyclo-phane Acta crystallographica. Section E, Structure reports online
17200923 2007-01-01 9-fluorenylphosphines for the Pd-catalyzed sonogashira, suzuki, and Buchwald-Hartwig coupling reactions in organic solvents and water Chemistry (Weinheim an der Bergstrasse, Germany)
15176842 2004-06-11 Stereoselective synthesis of atropisomeric korupensamines A and B utilizing planar chiral arene chromium complex The Journal of organic chemistry
12945899 2003-06-21 Suzuki-Miyaura homocoupling of naphthyl triflates using bis(pinacolato)diboron: approaches to the biaryl skeleton of crisamicin A Organic & biomolecular chemistry
12558411 2003-02-07 A new suzuki-heck-type coupling cascade: indeno[1,2,3]-annelation of polycyclic aromatic hydrocarbons The Journal of organic chemistry
12227814 2002-09-20 Synthesis and properties of a new member of the calixnaphthalene family: a C(2)-symmetrical endo-calix[4]naphthalene The Journal of organic chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Online Inquiry
  • Verification code
USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Copyright © 2024 BOC Sciences. All rights reserved.
Top
Inquiry Basket