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17640

Sigma-Aldrich

1-Bromonaphthalene

≥95%

Sinónimos:

1-Naphthyl bromide

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About This Item

Fórmula empírica (notación de Hill):
C10H7Br
Número de CAS:
90-11-9
Peso molecular:
207.07
Beilstein/REAXYS Number:
1906414
EC Number:
201-965-2
MDL number:
MFCD00003868
UNSPSC Code:
12352100
eCl@ss:
39060108
PubChem Substance ID:
57647656
NACRES:
NA.22

assay

≥95%

form

liquid

color

slightly yellow to deep brown-yellow

refractive index

n20/D 1.6570 (lit.)

bp

133-134 °C/10 mmHg (lit.)

mp

−2-−1 °C (lit.)

solubility

H2O: slightly soluble
alcohol: miscible
benzene: miscible
chloroform: miscible
diethyl ether: miscible

density

1.48 g/mL at 20 °C (lit.)

functional group

bromo

SMILES string

Brc1cccc2ccccc12

InChI

1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H

InChI key

DLKQHBOKULLWDQ-UHFFFAOYSA-N

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Categorías relacionadas

General description

The vibrational spectra of 1-bromonaphthalene has been studied.

Application

1-Bromonaphthalene was used as a solvent for the exfoliation and dispersion of hexabenzocoronene (HBC).

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
BCCM4240
BCCK3446
BCCL2355
BCCH9438
BCCH3693

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M Arivazhagan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 553-560 (2011-10-01)
In this work, the experimental and theoretical vibrational spectra of 1-bromonaphthalene (1-BN) were studied. FTIR and FT Raman spectra were recorded in the region 4000-400 cm(-1) and 3500-50 cm(-1), respectively. The structural and spectroscopic data of the molecule in the
Xinzhen Du et al.
Journal of colloid and interface science, 274(2), 645-651 (2004-05-18)
The binding of polyethylene glycol (10) n-octylphenyl ether (OPE) and polyethylene glycol (10) tert-octylphenyl ether (Triton X-100, TX) to beta-cyclodextrin (beta-CD) and heptakis(2,3- beta-dimethyl)- beta-CD (DM- beta-CD) was described in detail by surface tension, steady-state fluorescence of OPE and TX
Xin-zhen Du et al.
Guang pu xue yu guang pu fen xi = Guang pu, 24(4), 402-406 (2005-03-16)
Room-temperature phosphorescence of 1-BrN induced by a combination of OPE-10 and Triton X-100 with beta-CD was comparatively studied. In terms of molecular size and dimensions of beta-CD, the octyl group and phenyl group of OPE-10 and Triton X-100 were incorporated
J Marguerite Hughes et al.
Journal of the American Chemical Society, 134(29), 12168-12179 (2012-06-22)
We have studied the exfoliation and dispersion of hexabenzocoronene (HBC) in 28 different solvents. We see a wide range of dispersed concentrations and aggregation states, all of which can be related to the solvent properties. To a first approximation, the
Ya-Xian Zhu et al.
Analytica chimica acta, 583(2), 364-369 (2007-03-28)
Two novel heterocyclic third components, hexahydropyridine (HHP) and 1-ethylpiperidine (EP) were firstly found to enhance room temperature phosphorescence (RTP) of alpha-bromonaphthalene (alpha-BrN) induced by cyclodextrin. The effects of equilibrium time for formation of inclusion complex, temperature, pH values and the
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