ChemicalBook >> CAS DataBase List >>4-Chloro-8-aminoquinoline

4-Chloro-8-aminoquinoline

CAS No.
81764-16-1
Chemical Name:
4-Chloro-8-aminoquinoline
Synonyms
4-Chloroquinolin-8-aMine;4-Chloro-8-quinolylaMine;4-Chloro-8-aminoquinoline;8-Amino-4-chloroquinoline;8-Quinolinamine, 4-chloro-
CBNumber:
CB82537625
Molecular Formula:
C9H7ClN2
Molecular Weight:
178.62
MDL Number:
MFCD18448245
MOL File:
81764-16-1.mol
Last updated:2025-07-24 18:13:52
Product description Number Pack Size Price
4-Chloroquinolin-8-amine 95% OR931277 1g $135
4-Chloroquinolin-8-amine 95% 3H30-5-9W 1g $216
4-CHLOROQUINOLIN-8-AMINE 95.00% HCH0366222 5MG $501.42
4-Chloroquinolin-8-amine 95% OR931277 5g $555
4-Chloroquinolin-8-amine 2667AC 10g $563
More product size

4-Chloro-8-aminoquinoline Properties

Melting point 99-100 °C
Boiling point 333.7±27.0 °C(Predicted)
Density 1.363±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 2.65±0.13(Predicted)
Appearance White to light yellow Solid

SAFETY

Risk and Safety Statements

HS Code  2933499090

4-Chloro-8-aminoquinoline price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific OR931277 4-Chloroquinolin-8-amine 95% 81764-16-1 1g $135 2021-12-16 Buy
SynQuest Laboratories 3H30-5-9W 4-Chloroquinolin-8-amine 95% 81764-16-1 1g $216 2021-12-16 Buy
American Custom Chemicals Corporation HCH0366222 4-CHLOROQUINOLIN-8-AMINE 95.00% 81764-16-1 5MG $501.42 2021-12-16 Buy
Apolloscientific OR931277 4-Chloroquinolin-8-amine 95% 81764-16-1 5g $555 2021-12-16 Buy
AK Scientific 2667AC 4-Chloroquinolin-8-amine 81764-16-1 10g $563 2021-12-16 Buy
Product number Packaging Price Buy
OR931277 1g $135 Buy
3H30-5-9W 1g $216 Buy
HCH0366222 5MG $501.42 Buy
OR931277 5g $555 Buy
2667AC 10g $563 Buy

4-Chloro-8-aminoquinoline Chemical Properties,Uses,Production

Chemical Properties

Yellow solid

Synthesis

4-CHLORO-8-NITROQUINOLINE

23833-99-0

4-Chloro-8-aminoquinoline

81764-16-1

GENERAL METHOD: 4-Chloro-8-nitroquinoline (90 mg, 0.292 mmol) was dissolved in ethanol (2 mL) and iron powder (163 mg, 2.92 mmol) and ammonium chloride (127 mg, 2.33 mmol) were added sequentially. The reaction mixture was heated and refluxed for 2 hours. Upon completion of the reaction, the reaction mixture was filtered through diatomaceous earth and the diatomaceous earth bed was washed with a chloroform solution of 10% methanol. The filtrate was washed sequentially with saturated aqueous sodium bicarbonate solution and pure water. The organic layer was separated, dried over anhydrous sodium sulfate and filtered, and concentrated to give 70 mg of the target product 4-chloro-8-aminoquinoline. The product was confirmed by 1H NMR (300 MHz, DMSO-d6) and mass spectrometry (MS). Synthesis of 4-chloro-8-aminoquinoline: 200 mg of the target product was obtained by reaction using a mixed solution of ethanol (6 mL) and water (3 mL) of 4-chloro-8-nitroquinoline (250 mg, 1.20 mmol), ammonium chloride (513 mg, 9.60 mmol), and iron powder (671 mg, 12.0 mmol) according to the above general method. The product was confirmed by 1H NMR (400 MHz, CDCl3) and mass spectrometry (MS).

References

[1] Dalton Transactions, 2012, vol. 41, # 38, p. 11776 - 11782
[2] Journal of the American Chemical Society, 1947, vol. 69, p. 303,306
[3] Journal of the American Chemical Society, 1946, vol. 68, p. 1524,1526
[4] Patent: US2013/210844, 2013, A1. Location in patent: Paragraph 0322; 0517; 0518

4-Chloro-8-aminoquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

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4-Chloro-8-aminoquinoline Spectrum

4-Chloro-8-aminoquinoline 4-Chloro-8-quinolylaMine 4-Chloroquinolin-8-aMine 8-Quinolinamine, 4-chloro- 8-Amino-4-chloroquinoline 81764-16-1