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

2-AMINO-4-BROMOQUINOLINE

Product Name
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
Formula Weight
223.07
MOL File
36825-32-8.mol
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2-AMINO-4-BROMOQUINOLINE Property

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
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Safety

HS Code 
2933499090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

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

TRC
Product number
B292350
Product name
4-bromoquinolin-2-amine
Packaging
100mg
Price
$90
Updated
2021/12/16
AK Scientific
Product number
1229CV
Product name
4-Bromoquinolin-2-amine
Packaging
100mg
Price
$159
Updated
2021/12/16
SynQuest Laboratories
Product number
3H30-9-59
Product name
2-Amino-4-bromoquinoline
Packaging
100mg
Price
$208
Updated
2021/12/16
AK Scientific
Product number
1229CV
Product name
4-Bromoquinolin-2-amine
Packaging
250mg
Price
$240
Updated
2021/12/16
SynQuest Laboratories
Product number
3H30-9-59
Product name
2-Amino-4-bromoquinoline
Packaging
250mg
Price
$333
Updated
2021/12/16
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2-AMINO-4-BROMOQUINOLINE Chemical Properties,Usage,Production

Synthesis

42712-64-1

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 Suppliers

Apollo Scientific Ltd.
Tel
--
Fax
--
Email
sales@apolloscientific.co.uk
Country
United Kingdom
ProdList
6084
Advantage
88

36825-32-8, 2-AMINO-4-BROMOQUINOLINERelated 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