ChemicalBook >> CAS DataBase List >>2-AMINO-4-BROMOQUINOLINE

2-AMINO-4-BROMOQUINOLINE

CAS No.
36825-32-8
Chemical Name:
2-AMINO-4-BROMOQUINOLINE
Synonyms
4-Bromoquinolin-2-amine;4-Bromo-2-quinolinamine;2-AMINO-4-BROMOQUINOLINE;2-Quinolinamine, 4-bromo-;2-Amino-4-bromoquinoline 97%;4-Bromoquinolin-2-amine, 2-Amino-4-bromo-1-azanaphthalene
CBNumber:
CB8847397
Molecular Formula:
C9H7BrN2
Molecular Weight:
223.07
MDL Number:
MFCD00234500
MOL File:
36825-32-8.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:45
Product description Number Pack Size Price
4-bromoquinolin-2-amine B292350 100mg $90
4-Bromoquinolin-2-amine 1229CV 100mg $159
2-Amino-4-bromoquinoline 3H30-9-59 100mg $208
4-Bromoquinolin-2-amine 1229CV 250mg $240
2-Amino-4-bromoquinoline 3H30-9-59 250mg $333
More product size

2-AMINO-4-BROMOQUINOLINE Properties

Melting point 137-138℃
Boiling point 359℃
Density 1.649
Flash point 171℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 5.01±0.50(Predicted)
Appearance Light yellow to brown Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  2933499090

2-AMINO-4-BROMOQUINOLINE price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B292350 4-bromoquinolin-2-amine 36825-32-8 100mg $90 2021-12-16 Buy
AK Scientific 1229CV 4-Bromoquinolin-2-amine 36825-32-8 100mg $159 2021-12-16 Buy
SynQuest Laboratories 3H30-9-59 2-Amino-4-bromoquinoline 36825-32-8 100mg $208 2021-12-16 Buy
AK Scientific 1229CV 4-Bromoquinolin-2-amine 36825-32-8 250mg $240 2021-12-16 Buy
SynQuest Laboratories 3H30-9-59 2-Amino-4-bromoquinoline 36825-32-8 250mg $333 2021-12-16 Buy
Product number Packaging Price Buy
B292350 100mg $90 Buy
1229CV 100mg $159 Buy
3H30-9-59 100mg $208 Buy
1229CV 250mg $240 Buy
3H30-9-59 250mg $333 Buy

2-AMINO-4-BROMOQUINOLINE Chemical Properties,Uses,Production

Synthesis

2-AMINO-4-HYDROXYQUINOLINE HYDRATE

42712-64-1

2-AMINO-4-BROMOQUINOLINE

36825-32-8

The general procedure for the synthesis of 2-amino-4-bromoquinoline from 2-amino-4-hydroxyquinoline was as follows: 2-aminoquinolin-4-ol (0.7 g, 4.37 mmol) was added to a pressure tube, followed by phosphorus tribromide oxide (2.51 g, 8.74 mmol) and phosphorus tribromide (3 mL, 31.8 mmol). The pressure tube was sealed and the reaction was heated at 150°C for 19 hours under nitrogen protection. Upon completion of the reaction, the reaction mixture was cooled to room temperature, alkalized with 2 M aqueous sodium hydroxide (10 mL) and subsequently extracted with ethyl acetate (3 x 25 mL). The organic layers were combined, washed with water (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting solid was washed with hexane (20 mL) to remove non-polar impurities and dried under reduced pressure to give a dark brown residue. This residue was purified by silica gel column chromatography (using a gradient elution of methanol and chloroform) to give 4-bromoquinolin-2-amine (160 mg, 0.71 mmol, 16% yield). LC-MS (ESI) m/z 223.0 (bromine isotope mode) [(M + H)+, calculated value C9H8BrN2, 223.0]; LC-MS retention time (method B): tR = 1.14 min.

References

[1] Patent: WO2015/116492, 2015, A1. Location in patent: Page/Page column 105-106

2-AMINO-4-BROMOQUINOLINE Preparation Products And Raw materials

Raw materials

Preparation Products

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2-AMINO-4-BROMOQUINOLINE Spectrum

36825-32-8(2-AMINO-4-BROMOQUINOLINE)Related Search:

4-Bromoquinolin-2-amine 4-Bromo-2-quinolinamine 2-AMINO-4-BROMOQUINOLINE 2-Amino-4-bromoquinoline 97% 4-Bromoquinolin-2-amine, 2-Amino-4-bromo-1-azanaphthalene 2-Quinolinamine, 4-bromo- 36825-32-8