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2-HYDRAZINOQUINOLINE

Basic information Safety Supplier Related

2-HYDRAZINOQUINOLINE Basic information

Product Name:
2-HYDRAZINOQUINOLINE
Synonyms:
  • 2(1H)-Quinolinone, hydrazone
  • 2-hydrazinyl-2-oxo-N-[3-(trifluoromethyl)phenyl]acetamide
  • 2(1h)-quinolinone,hydrazone
  • alpha-Quinolylhydrazine
  • AKOS AUF02055
  • 2-HYDRAZINEQUINOLINE
  • 2-HYDRAZINOQUINOLINE
  • 2-QUINOLYLHYDRAZINE
CAS:
15793-77-8
MF:
C9H9N3
MW:
159.19
EINECS:
239-899-1
Product Categories:
  • Quinoline&Isoquinoline
  • Quinolinecarboxylic Acids, etc.
  • Quinolines
Mol File:
15793-77-8.mol
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2-HYDRAZINOQUINOLINE Chemical Properties

Melting point:
142°C
Boiling point:
303.1±45.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility 
Soluble in methanol.
pka
5.41±0.20(Predicted)
form 
powder to crystal
color 
Light yellow to Brown
CAS DataBase Reference
15793-77-8(CAS DataBase Reference)
EPA Substance Registry System
2(1H)-Quinolinone, hydrazone (15793-77-8)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38-41-22
Safety Statements 
26-36/37/39-39
TSCA 
Yes
HS Code 
2933491090

MSDS

  • Language:English Provider:ALFA
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2-HYDRAZINOQUINOLINE Usage And Synthesis

Uses

2-Hydrazinoquinoline acts as as a derivatization agent for LC-MS-based metabolomic investigation of diabetic ketoacidosis. It is used in agrochemical, pharmaceutical and dyestuff field.

Synthesis

612-62-4

15793-77-8

The general procedure for the synthesis of 2-hydrazinoquinoline from 2-chloroquinoline was as follows: 21.0 g (128.4 mmol) of 2-chloroquinoline was first dissolved in 210 mL of ethanol. Subsequently, 64.3 g (1.3 mol) of hydrazine hydrate was added and the reaction mixture was stirred under reflux conditions for 16 hours. Upon completion of the reaction, the mixture was cooled to 0 °C and the precipitated solid product was collected by filtration and washed with a small amount of ethanol. After initial drying, the product was further dried under high vacuum. Finally, 14.5 g of product was obtained in 71% yield. The product was analyzed by LC-MS (Method 1): retention time Rt = 1.95 min; mass spectrum (ESIpos): m/z = 160 [M + H]+; 1H-NMR (400 MHz, DMSO-d6) data were as follows: δ= 8.08 (broad peaks, 1H), 7.87 (double peaks, 1H), 7.63 (double peaks, 1H), 7.57-7.43 (multiple peaks, 2H), 7.16 (triple peaks, 1H), 6.85 (double peaks, 1H), 4.35 (broad peaks, 2H).

References

[1] Patent: US2012/264704, 2012, A1. Location in patent: Page/Page column 17
[2] Journal of the Chemical Society, 1913, vol. 103, p. 1981
[3] Journal of the Indian Chemical Society, 1981, vol. 58, p. 840 - 843
[4] Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2006, vol. 65, # 2, p. 463 - 466
[5] Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2007, vol. 66, # 4-5, p. 972 - 975

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