2-HYDRAZINOQUINOLINE
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
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)
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
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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