ChemicalBook--->CAS DataBase List--->7112-38-1

7112-38-1

7112-38-1 Structure

7112-38-1 Structure
IdentificationBack Directory
[Name]

PYRIDIN-3-YLMETHYL-HYDRAZINE
[CAS]

7112-38-1
[Synonyms]

PYRIDIN-3-YLMETHYL-HYDRAZINE
3-(hydrazinylMethyl)pyridine
Pyridine,3-(hydrazinylmethyl)-
1-(pyridin-3-ylmethyl)hydrazine
PYRIDIN-3-YLMETHYL-HYDRAZINE HCL
Pyridin-3-ylmethyl-hydrazine ,98%
[Molecular Formula]

C6H9N3
[MDL Number]

MFCD07786307
[MOL File]

7112-38-1.mol
[Molecular Weight]

123.16
Chemical PropertiesBack Directory
[Boiling point ]

310℃
[density ]

1.104
[Fp ]

141℃
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrogen-->HYDRAZINE
Spectrum DetailBack Directory
[Spectrum Detail]

PYRIDIN-3-YLMETHYL-HYDRAZINE(7112-38-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Pyridinecarboxaldehyde

500-22-1

PYRIDIN-3-YLMETHYL-HYDRAZINE

7112-38-1

General procedure for the synthesis of pyridine-3-methylidenehydrazine (1-(3-pyridyl)methylhydrazine) from 3-pyridinecarboxaldehyde: Hydrazine (1.05 mL, 46.7 mmol) was slowly added to a solution of methanol (100 mL) containing 3-pyridinecarboxaldehyde (5 g, 46.7 mmol). The reaction mixture was stirred continuously for 1 hour at room temperature. Subsequently, the air in the reaction system was replaced with nitrogen and 10% Pd/C catalyst (200 mg) was added. The nitrogen was again replaced with hydrogen and the reaction mixture was stirred overnight at room temperature under hydrogen atmosphere. Upon completion of the reaction, the solid catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to give the crude product pyridine-3-methylenehydrazine (Example 85A). This crude product can be used directly in the subsequent reaction without further purification. Yield: 5.2 g (91% yield). Mass spectrometry (DCI) analysis result: m/z 124 ([M+H]+).

[References]

[1] Patent: WO2007/95628, 2007, A1. Location in patent: Page/Page column 69-70
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