Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Quinoline compounds >  4-Chloro-3-nitroquinoline

4-Chloro-3-nitroquinoline

Basic information Safety Supplier Related

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
More
Less

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)
More
Less

Safety Information

Safety Statements 
24/25
HS Code 
29334900
More
Less

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-nitroquinolineSupplier

Changzhou Anchor Biological Technology Co., Ltd Gold
Tel
0519-85519868 18915088878
Email
sales@ankerbio.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18