4-Chloro-3-nitroquinoline
4-Chloro-3-nitroquinoline Basic information
- Product Name:
- 4-Chloro-3-nitroquinoline
- Synonyms:
-
- 4-Chloro-3-nitroquinoline ,98%
- 3-Nitro-4-chloroquinoline
- QUINOLINE, 4-CHLORO-3-NITRO-
- 4-CHLORO-3-NITROQUINOLINE
- 4-Chloro-3-nitroqulinoline
- 4-Chloro-3-nitroquinoline ISO 9001:2015 REACH
- CAS:
- 39061-97-7
- MF:
- C9H5ClN2O2
- MW:
- 208.6
- EINECS:
- 1533716-785-6
- Product Categories:
-
- pharmacetical
- Quinoline&Isoquinoline
- API intermediates
- Aromatics Compounds
- Quinoline
- Aromatics
- Heterocycles
- Intermediates
- Mol File:
- 39061-97-7.mol
4-Chloro-3-nitroquinoline Chemical Properties
- Melting point:
- 121-122°C
- Boiling point:
- 333.8±22.0 °C(Predicted)
- Density
- 1.484±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- -0.28±0.24(Predicted)
- color
- Pale Yellow
- InChI
- InChI=1S/C9H5ClN2O2/c10-9-6-3-1-2-4-7(6)11-5-8(9)12(13)14/h1-5H
- InChIKey
- ZRFUZDDJSQVQBY-UHFFFAOYSA-N
- SMILES
- N1C2C(=CC=CC=2)C(Cl)=C([N+]([O-])=O)C=1
- CAS DataBase Reference
- 39061-97-7(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29334900
4-Chloro-3-nitroquinoline Usage And Synthesis
Chemical Properties
yellow crystal powder
Uses
4-Chloro-3-nitroquinoline (cas# 39061-97-7) is a compound useful in organic synthesis.
Synthesis
50332-66-6
39061-97-7
General procedure for the synthesis of 4-chloro-3-nitroquinoline from 4-hydroxy-3-nitroquinoline: The intermediate 3-nitro-4-hydroxyquinoline (18.7 g, 98.4 mmol) was suspended in dichloromethane (150 mL). Thionyl chloride (17.2 mL, 236 mmol) and N,N-dimethylformamide (DMF, 9.2 mL, 118 mmol) were added sequentially to the suspension. The reaction mixture was heated to reflux and kept reacting overnight. Upon completion of the reaction, the mixture was slowly poured into ice water. The organic and aqueous layers were separated and the organic layer was washed sequentially with saturated sodium bicarbonate solution, water and saturated brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue (20.52 g, 93% yield) can be used directly in the subsequent reaction without further purification.
References
[1] Patent: EP2674170, 2013, A1. Location in patent: Paragraph 0228
[2] Patent: US2014/141033, 2014, A1. Location in patent: Page/Page column
[3] Journal of Medicinal Chemistry, 1991, vol. 34, # 3, p. 1202 - 1206
[4] Journal of Medicinal Chemistry, 2006, vol. 49, # 11, p. 3354 - 3361
[5] Patent: WO2007/89507, 2007, A1. Location in patent: Page/Page column 20-21
4-Chloro-3-nitroquinoline Preparation Products And Raw materials
Raw materials
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