ChemicalBook > CAS DataBase List > 1-Bromonaphthalene

1-Bromonaphthalene

Product Name
1-Bromonaphthalene
CAS No.
90-11-9
Chemical Name
1-Bromonaphthalene
Synonyms
1-Bromonaphtalene;1-Naphthyl bromide;α-bromonaphthalene;1-BromonaphthaL;I-Bromnaphthalin;1-Bromnaphthalin;1-Naphtyl bromide;1-BreMnaphthalene;1-naphthylbromide;-Bromonaphthalene
CBNumber
CB5197277
Molecular Formula
C10H7Br
Formula Weight
207.07
MOL File
90-11-9.mol
More
Less

1-Bromonaphthalene Property

Melting point:
−2-−1 °C(lit.)
Boiling point:
133-134 °C10 mm Hg(lit.)
Density 
1.48 g/mL at 20 °C(lit.)
vapor pressure 
0.013 hPa (20 °C)
refractive index 
n20/D 1.6570(lit.)
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
H2O: slightly soluble
form 
Liquid
color 
slightly yellow to deep brownish-yellow
Water Solubility 
slightly soluble
Merck 
14,1425
BRN 
1906414
Dielectric constant
5.1(19℃)
InChIKey
DLKQHBOKULLWDQ-UHFFFAOYSA-N
LogP
4.06
CAS DataBase Reference
90-11-9(CAS DataBase Reference)
NIST Chemistry Reference
Naphthalene, 1-bromo-(90-11-9)
EPA Substance Registry System
Naphthalene, 1-bromo- (90-11-9)
More
Less

Safety

Hazard Codes 
Xn,Xi
Risk Statements 
22-36-36/37/38-20/21/22
Safety Statements 
26-36
RIDADR 
2810
WGK Germany 
3
RTECS 
QJ1545000
8
TSCA 
Yes
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29036990
Toxicity
LD50 orally in Rabbit: 810 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H319Causes serious eye irritation

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.06210
Product name
1-Bromonaphthalene
Purity
for synthesis
Packaging
100mL
Price
$70
Updated
2024/03/01
Sigma-Aldrich
Product number
8.06210
Product name
1-Bromonaphthalene
Purity
for synthesis
Packaging
500mL
Price
$312
Updated
2024/03/01
Sigma-Aldrich
Product number
8.06210
Product name
1-Bromonaphthalene
Purity
for synthesis
Packaging
2.5L
Price
$1400
Updated
2024/03/01
Sigma-Aldrich
Product number
17640
Product name
1-Bromonaphthalene
Purity
≥95%
Packaging
100ml
Price
$127
Updated
2024/03/01
Sigma-Aldrich
Product number
17640
Product name
1-Bromonaphthalene
Purity
≥95%
Packaging
500ml
Price
$371
Updated
2024/03/01
More
Less

1-Bromonaphthalene Chemical Properties,Usage,Production

Chemical Properties

Thick colorless yellow to yellow-brown liquid with a pungent odor. Insoluble in water, miscible with alcohol, ether, benzene and chloroform. 1-Bromonaphthalene is one of two isomeric bromonaphthalenes, the other being 2-bromonaphthalene.

Uses

1-Bromonaphthalene is used in organic synthesis and refractometry of fats. It is used in the preparation of N-aryl imidazoles and diaryl ethers. It is used to determine the refractive index of crystals and the water content of alcohols. It is utilized in the preparation of glutathione peroxidase-like antioxidant activity of diaryl diselenides. Further, it serves as a solvent for the exfoliation and dispersion of hexabenzocoronene. In addition to this, it is used as a refrigerant and a solvent molecular weight substance.

Preparation

1-Bromonaphthalene is synthesized by the reaction of naphthalene with bromine: C10H8+ Br2→ C10H7Br + HBr.
Reaction: add carbon tetrachloride and naphthalene in the reaction pot, stirring and heating, and slowly add bromine at 45℃. After adding, keep the reaction at 70-80℃ for 3-4h. distillation to recover carbon tetrachloride, wash the reaction product, distill under reduced pressure, wash again, filter, dry and get the finished product.

Application

1-Bromonaphthalene is a bromoarene that can be used in:
Palladium-catalyzed Suzuki–Miyaura coupling reaction with potassium aryltrifluoroborates without the use of phase-transfer catalysts or phosphine ligands.
The preparation of indeno annelated polycyclic aromatic hydrocarbons by reacting with o-bromobenzeneboronic acid and oligocyclic bromoarenes via Suzuki-Heck type coupling.
Ni catalyzed Kumada–Tamao–Corriu cross-coupling reaction with PhMgBr.
The preparation of arylnaphthalenes via palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with aryl boronic acid.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 1, p. 121, 1941
Tetrahedron, 64, p. 4999, 2008 DOI: 10.1016/j.tet.2008.03.085

General Description

The vibrational spectra of 1-bromonaphthalene has been studied.

Purification Methods

Purify 1-bromonaphthalene by passage through activated alumina, and three vacuum distillations. [Beilstein 5 H 547, 5 IV 1665.]

More
Less

1-Bromonaphthalene Suppliers

Changzhou Zhongji Chemical Co.,Ltd
Tel
0519-85156279-811,812
Fax
0519-85156279-816
Email
sales@czzjchem.com
Country
China
ProdList
20
Advantage
58
Guangdong wengjiang Chemical Reagent Co., Ltd.
Tel
0751-2886750 13927877953
Fax
0751-2886750
Email
3005811397@qq.com
Country
China
ProdList
13374
Advantage
58
Shaanxi tuoyu Xinghua Technology Co., Ltd
Tel
13892521602
Fax
0913-2123492
Email
3216966844@qq.com
Country
China
ProdList
32
Advantage
58
Weifang Siyuan Chemical Co., Ltd.
Tel
0536-8888106 17663601818
Fax
0536-8888106
Email
2354379876@qq.com
Country
China
ProdList
244
Advantage
58
Shaanxi wopin Chemical Technology Co., Ltd
Tel
18792798662
Email
3120382920@qq.com
Country
China
ProdList
179
Advantage
58
Pingdingshan Longwei Biotechnology Co. , Ltd.
Tel
15343756688
Email
3079249712@qq.com
Country
China
ProdList
316
Advantage
58
Inner Mongolia Yida Chemical Technology Co., Ltd.
Tel
18967392038
Email
67247734@qq.com
Country
China
ProdList
74
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
INTATRADE GmbH
Tel
+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
ProdList
3576
Advantage
66
More
Less

View Lastest Price from 1-Bromonaphthalene manufacturers

Speranza Chemical Co., Ltd.
Product
1-Bromonaphthalene 90-11-9
Price
US $15.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
200 tons/ year
Release date
2020-03-11
Shanghai Qyubiotech Co., Ltd.
Product
1-Bromonaphthalene 90-11-9
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%+
Supply Ability
1000000kg per Month
Release date
2022-10-11
Henan Fengda Chemical Co., Ltd
Product
1-Bromonaphthalene 90-11-9
Price
US $200.00-1.00/KG
Min. Order
1KG
Purity
99%, 99.5% Sublimated
Supply Ability
g-kg-tons, free sample is available
Release date
2023-12-31

90-11-9, 1-BromonaphthaleneRelated Search:


  • 1-bromo-naphthalen
  • 1-Naphthyl bromide
  • A-BROMONAPHTHALENE
  • ALPHA-BROMONAPHTHALENE
  • ALPHA-MONOBROMONAPHTHALENE
  • ALPHA-NAPHTHYL BROMIDE
  • 1-BROMONAPHTHALENE
  • 1-BROMO NAPTHALENE
  • 1-Bromonaphtalene
  • 1-Bromonaphthalene solution
  • 1-BROMONAPHTHALENE STABILIZED
  • 1-BROMONAPHTHALENE SOLUTION, IN PARAFFIN OIL
  • 1-BromonaphthaleneForSynthesis
  • 1-Bromonaphthalene96%
  • 1-Bromonaphthalene,~99%
  • 1-Bromonaphthalene,97%
  • a-Naphthyl bromide
  • 1-Naphtyl bromide
  • 1-Bromonaphthalene ,98%
  • 1-BreMnaphthalene
  • 1-BroMonaphthalene, 96% 100ML
  • 1-naphthylbromide
  • -Bromonaphthalene
  • I-Bromnaphthalin
  • Naphthalene,1-bromo-
  • α-bromonaphthalene
  • 11 -BroMonaphthalene
  • 1 - broMine naphthalene
  • 1-Bromonaphthalene &gt
  • 1-BromonaphthaL
  • 1-Bromonaphthalene ISO 9001:2015 REACH
  • 1-Bromonaphthalene pure, 98%
  • 1-Bromonaphthalene, Extra Pure, SLR, Fisher Chemical
  • 1-Bromnaphthalin
  • 90-11-9
  • 33186
  • 1990-11-9
  • 99-11-9
  • 1990-11-09
  • 90119
  • ARYL HALIDE
  • Building Blocks
  • C9 to C12
  • Aryl
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Naphthalene series
  • Pyridines ,Heterocyclic Acids
  • C9 to C12
  • Chemical Synthesis
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Building Blocks
  • Naphthalene derivatives
  • Aryl
  • C9 to C12
  • Halogenated Hydrocarbons
  • Aromatic Compounds