N257
Naphthalene-1-boronic acid
≥95.0%
Synonym(s):
α-Naphthaleneboronic acid, α-Naphthylboronic acid, 1-Naphthaleneboronic acid, 1-Naphthylboronic acid, 1-naphthalenyl-boronic acid, NSC 78936
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About This Item
Linear Formula:
C10H7B(OH)2
CAS Number:
Molecular Weight:
171.99
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2937504
InChI
1S/C10H9BO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7,12-13H
SMILES string
OB(O)c1cccc2ccccc12
InChI key
HUMMCEUVDBVXTQ-UHFFFAOYSA-N
assay
≥95.0%
form
crystals
mp
208-214 °C (lit.)
Quality Level
Related Categories
Application
Naphthalene-1-boronic acid can be used:
- Methyl 5-bromo-2-(naphthalene-1-yl)benzoate, which is a starting material for the preparation of 9-anthracene-spirobenzofluorene host materials.
- A bifunctional polymer used for the hydrolysis of cellulose.
- 9-(Naphthalene-1-yl)anthracene, which is a key intermediate for the preparation of anthracene derived molecular glass having blue emission.
Other Notes
Contains varying amounts of anhydride
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Highly efficient blue OLED based on 9-anthracene-spirobenzofluorene derivatives as host materials
Gong M, et al.
Journal of Materials Chemistry, 20(47), 10735-10746 (2010)
Suzuki homo-coupling reaction based fluorescent sensors for monosaccharides
Xu S, et al.
Royal Society of Chemistry Advances, 4(66), 35238-35241 (2014)
Bifunctional porous polymers bearing boronic and sulfonic acids for hydrolysis of cellulose
Yang Q and Pan X
ACS sustainable chemistry & engineering, 4(9), 4824-4830 (2016)
Highly efficient and stable deep-blue emitting anthracene-derived molecular glass for versatile types of non-doped OLED applications
Cho I, et al.
Journal of Materials Chemistry, 22(1), 123-129 (2012)
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