Bromoquinoline Application and synthesis method Uses
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3-Bromoquinoline

Bromoquinoline Application and synthesis method Uses
Product Name
3-Bromoquinoline
CAS No.
5332-24-1
Chemical Name
3-Bromoquinoline
Synonyms
Quinoline, 3-bromo-;NSC 3995;CETH-016;3-BromoquinoL;Bromoquinoline;3-BROMOQUINOLINE;3-BROMOQUINLIINE;3-bromo-quinolin;3-Bromoquuinoline;1-3-Bromoquinoline
CBNumber
CB4220082
Molecular Formula
C9H6BrN
Formula Weight
208.05
MOL File
5332-24-1.mol
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3-Bromoquinoline Property

Melting point:
13-15 °C (lit.)
Boiling point:
274-276 °C (lit.)
Density 
1.533 g/mL at 25 °C (lit.)
vapor pressure 
0.196Pa at 25℃
refractive index 
n20/D 1.664(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
2.69(at 25℃)
form 
Liquid
color 
Clear colorless to yellow
Water Solubility 
103mg/L at 25℃
BRN 
112939
InChI
1S/C9H6BrN/c10-8-5-7-3-1-2-4-9(7)11-6-8/h1-6H
InChIKey
ZGIKWINFUGEQEO-UHFFFAOYSA-N
SMILES
Brc1cnc2ccccc2c1
LogP
3.03
CAS DataBase Reference
5332-24-1(CAS DataBase Reference)
NIST Chemistry Reference
Quinoline, 3-bromo-(5332-24-1)
EPA Substance Registry System
Quinoline, 3-bromo- (5332-24-1)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
RIDADR 
UN2810
WGK Germany 
3
TSCA 
TSCA listed
HS Code 
29334900
Storage Class
10 - Combustible liquids
Hazard Classifications
Eye Irrit. 2
Skin Irrit. 2
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
124133
Product name
3-Bromoquinoline
Purity
98%
Packaging
25g
Price
$123
Updated
2025/07/31
Sigma-Aldrich
Product number
124133
Product name
3-Bromoquinoline
Purity
98%
Packaging
100g
Price
$230.3
Updated
2025/07/31
TCI Chemical
Product number
B1013
Product name
3-Bromoquinoline
Purity
>98.0%(GC)(T)
Packaging
25g
Price
$93
Updated
2025/07/31
TRC
Product number
B686875
Product name
3-Bromoquinoline
Packaging
25g
Price
$70
Updated
2021/12/16
Frontier Specialty Chemicals
Product number
JK261772
Product name
3-Bromoquinoline
Packaging
25g
Price
$76
Updated
2021/12/16
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3-Bromoquinoline Chemical Properties,Usage,Production

Bromoquinoline

There are seven position isomers with the main properties are as follows:

Name
Melting point(℃)
Boiling point(℃)
Solubility
2-bromoquinoline
48~49
It is soluble in diethyl ether, chloroform and benzene
3-bromoquinoline
12~15
274~276, 95(66.66Pa)
4-bromoquinoline
29~30
270(decomposition)
Easily soluble in dilute acid
5-bromoquinoline
52 (needle crystal)
280
6-bromoquinoline
24
278
7-bromoquinoline
52 (needle crystal)
290
8-bromoquinoline
80
165~166
(2399.79Pa)

Application and synthesis method

3-Bromoquinoline can have action with mixed acid to generate 3-bromo-5-nitroquinoline, followed by heating with potassium permanganate to be oxidized to 5-bromo-2, 3-pyridine dicarboxylic acid.
6-bromo-quinoline can be heated together nitric acid to generate 6-bromo-8-nitro-quinoline, followed by reaction with potassium permanganate to be oxidized into 2, 3-pyridinedicarboxylic acid.
2-bromo-quinoline can be manufactured through the reaction between 2-hydroxyquinoline and phosphorus pentabromide
3-bromo-quinoline can be obtained through heating the quinoline perbromide at 180 ° C.
4-bromoquinoline can be obtained through either the heating reaction between 4-hydroxyquinoline and phosphorus pentabromide or by the diazotization reaction of 4-aminoquinoline.
5-bromo-quinoline can be obtained from the heating reaction between m-bromo aniline, glycerol, m-bromonitrobenzene and concentrated sulfuric acid, or through the diazotization reaction of 5-amino-quinoline.
6-bromo-quinoline can be obtained through the heating reaction between p-bromoaniline, glycerol, concentrated sulfuric acid and p-bromo-nitrobenzene.
7-bromoquinoline can be obtained through the diazotization of 7-aminoquinoline.
8-bromo-quinoline can be obtained through the heating of o-bromo aniline, glycerol, concentrated sulfuric acid and o-bromo-nitrobenzene in the heating system.
Purposes: as organic synthesis reagents.

Uses

For pharmaceuticals
Medicine, pesticide intermediates

Chemical Properties

colorless to light yellow liquid

Uses

3-Bromoquinoline undergoes bromine-magnesium exchange reaction with lithium tributylmagnesate in toluene at -10°C, which is quenched by various electrophiles to yield functionalized quinolines.

Synthesis Reference(s)

The Journal of Organic Chemistry, 27, p. 1318, 1962 DOI: 10.1021/jo01051a047

General Description

3-Bromoquinoline undergoes bromine-magnesium exchange reaction with lithium tributylmagnesate in toluene at -10°C, which is quenched by various electrophiles to yield functionalized quinolines.

Flammability and Explosibility

Not classified

References

[1] Patent: US3956301, 1976, A
[2] Patent: US5266700, 1993, A

3-Bromoquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

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3-Bromoquinoline Suppliers

Hefei Jiete Pharmaceutical Technology Co., Ltd
Tel
0551-18256521115 18256521115
Email
2788434637@qq.com
Country
China
ProdList
31
Advantage
58
Hubei zhonglong Kangsheng Fine Chemical Co., Ltd
Tel
027-83850381 18171045381
Email
2533797015@qq.com
Country
China
ProdList
974
Advantage
58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
INTATRADE GmbH
Tel
+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
ProdList
3572
Advantage
66
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Fax
86-027-87531808
Email
sales@chemwish.com
Country
China
ProdList
35896
Advantage
56
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Fax
0086-571-85864795
Country
China
ProdList
18207
Advantage
66
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View Lastest Price from 3-Bromoquinoline manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
3-Bromoquinoline 5332-24-1
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1Ton
Release date
2022-10-12
Shanghai UCHEM Inc.
Product
3-Bromoquinoline 5332-24-1
Price
US $11.00-119.00/g
Min. Order
25g
Purity
0.98
Supply Ability
25kg
Release date
2023-12-14
Hebei Zhanyao Biotechnology Co. Ltd
Product
3-Bromoquinoline 5332-24-1
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20 Tons
Release date
2021-10-13

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