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ChemicalBook--->CAS DataBase List--->72790-89-7

72790-89-7

72790-89-7 Structure

72790-89-7 Structure
IdentificationBack Directory
[Name]

1-METHYLCYCLOPROPANECARBOHYDRAZIDE
[CAS]

72790-89-7
[Synonyms]

1-METHYLCYCLOPROPANECARBOHYDRAZIDE
1-methylcyclopropane-1-carbohydrazide
1-METHYLCYCLOPROPANECARBOXYLIC ACID HYDRAZIDE
[Molecular Formula]

C5H10N2O
[MDL Number]

MFCD08061554
[MOL File]

72790-89-7.mol
[Molecular Weight]

114.15
Chemical PropertiesBack Directory
[Melting point ]

72-74 °C
[Boiling point ]

260.5±7.0 °C(Predicted)
[density ]

1.154±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

13.46±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H228-H302-H315-H319-H335
[Precautionary statements ]

P210-P240-P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P370+P378-P403+P233-P501
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHYLCYCLOPROPANECARBOHYDRAZIDE(72790-89-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL 1-METHYLCYCLOPROPANE-1-CARBOXYLATE

71441-76-4

1-METHYLCYCLOPROPANECARBOHYDRAZIDE

72790-89-7

The general procedure for the synthesis of 1-methylcyclopropane carbohydrazide from ethyl 1-methylcyclopropane-1-carboxylate is as follows: with reference to Example 2, 1-methyl-1-cyclopropane carbohydrazide was prepared as follows: 1-methyl-1-cyclopropane carbohydrazide ethyl ester (10 g, 7.8 mmol) was mixed with hydrazine monohydrate (5.1 g, 0.1 mol), and reacted with stirring and heating for 4 hr. at 100°C. . Subsequently, toluene (50 ml) was added to the reaction system and the mixture was refluxed for 3 h, during which the water generated was removed by azeotropic distillation. Upon completion of the reaction, the reaction was cooled to room temperature, the precipitated crystals were collected by filtration and washed with diisopropyl ether to give the final target product 1-methyl-1-cyclopropanecarbohydrazide (8.9 g) as colorless crystals. The yield was 99%, and the melting point was 85°-87°C. The product was obtained as a colorless crystal.

[References]

[1] Patent: US5367078, 1994, A
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