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MilliporeSigma

N257

Sigma-Aldrich

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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5 G
$42.90
25 G
$59.00

About This Item

Linear Formula:
C10H7B(OH)2
CAS Number:
Molecular Weight:
171.99
Beilstein/REAXYS Number:
2937504
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

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Quality Level

assay

≥95.0%

form

crystals

mp

208-214 °C (lit.)

SMILES string

OB(O)c1cccc2ccccc12

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

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1 of 4

This Item
480134B75956499978
assay

≥95.0%

assay

≥95.0%

assay

≥95.0%, 95%

assay

≥95%

mp

208-214 °C (lit.)

mp

269-275 °C (lit.)

mp

284-288 °C (lit.)

mp

256-260 °C (lit.)

form

crystals

form

-

form

crystals

form

-

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

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.[1]
  • A bifunctional polymer used for the hydrolysis of cellulose.[2]
  • 9-(Naphthalene-1-yl)anthracene, which is a key intermediate for the preparation of anthracene derived molecular glass having blue emission.[3]
It can also be as a substrate in fluorometric boronic acid based saccharide sensors based on the Suzuki homocoupling reactions.[4]

Other Notes

Contains varying amounts of anhydride

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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