4-BROMO-2-METHYLQUINOLINE
Uses- Product Name
- 4-BROMO-2-METHYLQUINOLINE
- CAS No.
- 50488-44-3
- Chemical Name
- 4-BROMO-2-METHYLQUINOLINE
- Synonyms
- 4-Bromoquinaldine;4-BROMO-2-METHYLQUINOLINE;2-Methyl-4-broMoquinoline;Quinoline, 4-bromo-2-methyl-;4-Bromo-2-methylquinoline 97%min;4-BROMO-2-METHYLQUINOLINE ISO 9001:2015 REACH
- CBNumber
- CB9846711
- Molecular Formula
- C10H8BrN
- Formula Weight
- 222.08
- MOL File
- 50488-44-3.mol
4-BROMO-2-METHYLQUINOLINE Property
- Boiling point:
- 88-90℃ (1 Torr)
- Density
- 1.488±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 4.21±0.50(Predicted)
- Appearance
- Yellow to brown Solid
Safety
- HS Code
- 2933499090
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
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
N-Bromosuccinimide Price
- Product number
- B697683
- Product name
- 4-Bromo-2-methylquinoline
- Packaging
- 100mg
- Price
- $65
- Updated
- 2021/12/16
- Product number
- FB142712
- Product name
- 4-Bromo-2-methylquinoline
- Packaging
- 250mg
- Price
- $100
- Updated
- 2021/12/16
- Product number
- Z4806
- Product name
- 4-Bromo-2-methylquinoline
- Packaging
- 250mg
- Price
- $114
- Updated
- 2021/12/16
- Product number
- FB142712
- Product name
- 4-Bromo-2-methylquinoline
- Packaging
- 500mg
- Price
- $150
- Updated
- 2021/12/16
- Product number
- FB142712
- Product name
- 4-Bromo-2-methylquinoline
- Packaging
- 1g
- Price
- $200
- Updated
- 2021/12/16
4-BROMO-2-METHYLQUINOLINE Chemical Properties,Usage,Production
Uses
4-Bromo-2-methylquinoline belongs to the quinoline class of organic compounds and can be used as a pharmaceutical intermediate. Literature reports that it can be used to prepare a class of carboxylic acid-substituted (hetero)aromatic ring derivatives with dual inhibitory activity against xanthine oxidase and URAT1, such as 4-(2-cyanoquinoline-4-yl)-2-hydroxybenzoic acid.
Synthesis
607-67-0
50488-44-3
(4a) 4-Hydroxy-2-methylquinoline (17.4 g, 109 mmol) and phosphorus oxyfluoride (47.1 g, 164 mmol) were added in a round bottom flask. The reaction mixture was heated to 130 °C and maintained for several hours. After completion of the reaction, it was cooled to room temperature and the residue was partitioned between saturated Na2CO3 solution and ethyl acetate. The organic layer was separated and the aqueous layer was extracted with ethyl acetate (5 × 300 mL). The organic layers were combined, washed sequentially with H2O (2 × 400 mL) and brine (1 × 400 mL), and dried with anhydrous MgSO4. After filtration, the filtrate was concentrated and the residue was purified by silica gel column chromatography to afford 4-bromo-2-methylquinoline (8.8 g, 36% yield).
References
[1] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 7, p. 1865 - 1870
[2] Patent: US2003/229084, 2003, A1. Location in patent: Page/Page column 33
[3] Patent: WO2017/36404, 2017, A1. Location in patent: Page/Page column 130
[4] Patent: EP96214, 1991, B1
[5] European Journal of Medicinal Chemistry, 2013, vol. 69, p. 527 - 536
4-BROMO-2-METHYLQUINOLINE Preparation Products And Raw materials
Raw materials
Preparation Products
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