8-CHLORO-3-IODOQUINOLINE
- Product Name
- 8-CHLORO-3-IODOQUINOLINE
- CAS No.
- 847727-21-3
- Chemical Name
- 8-CHLORO-3-IODOQUINOLINE
- Synonyms
- 8-CHLORO-3-IODOQUINOLINE;Quinoline, 8-chloro-3-iodo-
- CBNumber
- CB82455567
- Molecular Formula
- C9H5ClIN
- Formula Weight
- 289.5
- MOL File
- 847727-21-3.mol
8-CHLORO-3-IODOQUINOLINE Property
- storage temp.
- 2-8°C(protect from light)
- Appearance
- Light yellow to yellow Solid
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.
N-Bromosuccinimide Price
- Product number
- HCH0361532
- Product name
- 8-CHLORO-3-IODOQUINOLINE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $501.93
- Updated
- 2021/12/16
- Product number
- 116092
- Product name
- 8-Chloro-3-iodoquinoline
- Purity
- >97%
- Packaging
- 500mg
- Price
- $676
- Updated
- 2021/12/16
- Product number
- 9427BB
- Product name
- 8-Chloro-3-iodoquinoline
- Packaging
- 250mg
- Price
- $104
- Updated
- 2021/12/16
- Product number
- A117544
- Product name
- 8-Chloro-3-iodoquinoline
- Purity
- 97%
- Packaging
- 5g
- Price
- $293
- Updated
- 2021/12/16
- Product number
- 847727213
- Product name
- 8-Chloro-3-iodoquinoline
- Packaging
- 1g
- Price
- $400.05
- Updated
- 2021/12/16
8-CHLORO-3-IODOQUINOLINE Chemical Properties,Usage,Production
Synthesis
611-33-6
847727-21-3
8-Chloro-3-iodoquinoline (D1) was synthesized as follows: under argon protection, N-iodosuccinimide (67.9 g, 0.30 mmol) was added batchwise to a stirred solution of 8-chloroquinoline (49 g, 0.30 mmol) in acetic acid (300 mL). The reaction mixture was heated to 70 °C and kept for 18 hours. After completion of the reaction, the mixture was concentrated under vacuum. The residue was dissolved in dichloromethane (600 mL) and washed sequentially with 10% aqueous sodium thiosulfate (2 x 300 mL) and 10% aqueous sodium bicarbonate (2 x 300 mL). The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated in vacuum to obtain the crude product. The crude product was recrystallized with ethyl acetate to give the title compound (D1) as a yellow solid (42 g, 0.145 mol, 48% yield). The recrystallized residue was further purified by silica gel column chromatography using a gradient elution with toluene/acetone to give the second product (18 g, 69% total yield).
References
[1] Organic Letters, 2015, vol. 17, # 18, p. 4408 - 4411
[2] Journal of Medicinal Chemistry, 2014, vol. 57, # 9, p. 3884 - 3890
[3] Patent: WO2005/21530, 2005, A1. Location in patent: Page/Page column 12
[4] Patent: WO2005/30724, 2005, A1. Location in patent: Page/Page column 10-11
[5] Patent: WO2007/39219, 2007, A1. Location in patent: Page/Page column 29-30
8-CHLORO-3-IODOQUINOLINE Preparation Products And Raw materials
Raw materials
Preparation Products
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