4-Amino-6-bromoquinoline
- Product Name
- 4-Amino-6-bromoquinoline
- CAS No.
- 65340-73-0
- Chemical Name
- 4-Amino-6-bromoquinoline
- Synonyms
- 6-Bromoquinolin-4-amine;BUTTPARK 44\09-54;6-bromo-4-quinolinamine;4-AMINO-6-BROMOQUINOLINE;4-Quinolinamine, 6-bromo-;6-BROMO-QUINOLIN-4-YLAMINE;4-Amino-6-bromoquinoline ISO 9001:2015 REACH
- CBNumber
- CB2744087
- Molecular Formula
- C9H7BrN2
- Formula Weight
- 223.07
- MOL File
- 65340-73-0.mol
4-Amino-6-bromoquinoline Property
- Melting point:
- 228-230°C
- Boiling point:
- 388.7±27.0 °C(Predicted)
- Density
- 1.649±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- form
- solid
- pka
- 8.21±0.50(Predicted)
- Appearance
- White to yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H301Toxic if swalloed
H319Causes serious eye irritation
- Precautionary statements
-
P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- BBO000153
- Product name
- 4-Amino-6-bromoquinoline
- Purity
- Aldrich
- Packaging
- 1g
- Price
- $330
- Updated
- 2025/07/31
- Product number
- A594840
- Product name
- 4-Amino-6-bromoquinoline
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- FA50975
- Product name
- 4-Amino-6-bromoquinoline
- Packaging
- 100mg
- Price
- $89
- Updated
- 2021/12/16
- Product number
- Z4998
- Product name
- 4-Amino-6-bromoquinoline
- Packaging
- 250mg
- Price
- $111
- Updated
- 2021/12/16
- Product number
- FA50975
- Product name
- 4-Amino-6-bromoquinoline
- Packaging
- 250mg
- Price
- $130
- Updated
- 2021/12/16
4-Amino-6-bromoquinoline Chemical Properties,Usage,Production
Synthesis
65340-70-7
65340-73-0
The general procedure for the synthesis of 4-amino-6-bromoquinoline from 6-bromo-4-chloroquinoline was as follows: 6-bromo-4-chloroquinoline (500 mg, 2.1 mmol), acetamide (2.438 g, 41.3 mmol), and potassium carbonate (1.449 g, 10.5 mmol) were added to a reaction flask fitted with a magnetic stirrer. The reaction mixture was heated to 180 °C and maintained at this temperature for 5 hours. After completion of the reaction, the mixture was cooled to room temperature and diluted with water (50 mL). The aqueous phase was extracted with ethyl acetate (20 mL × 3), the organic phases were combined and dried over anhydrous sodium sulfate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: dichloromethane/methanol = 20:1) to afford the target product 6-bromoquinolin-4-amine (198 mg, 43% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6) and LC-MS (ESI) to confirm its structure.1H NMR (400 MHz, DMSO-d6) δ 8.46 (d, J = 2.2 Hz, 1H), 8.25 (d, J = 7.2 Hz, 1H), 7.95 (dd, J = 8.9, 2.3 Hz, 1H), 7.69 (d, J = 8.9, 2.3 Hz, 1H), 7.69 (d, J = 8.9, 2.3 Hz, 1H), 7.95 (dd, J = 8.9, 2.3 Hz, 2.3 Hz, 1H) 7.69 (d, J = 8.9 Hz, 1H), 7.12 (d, J = 7.2 Hz, 1H), 5.64 (s, 2H). LC-MS (ESI) m/z = 223.1, 225.1 (M + H, M + 2 + H).
References
[1] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 9, p. 1919 - 1922
4-Amino-6-bromoquinoline Preparation Products And Raw materials
Raw materials
Preparation Products
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