1-Methylcyclopropanecarbohydrazide

1-Methylcyclopropanecarbohydrazide Suppliers list
Company Name: Nantong MYBio-pharm. Co., Ltd.  
Tel: 0513-85921823 18662920231
Email: sales@ntminyanmedical.com
Company Name: Beijing FYF Chemicals Co., Ltd  
Tel: 010-57903446 15869909019
Email: 168931144@qq.com
Company Name: JW & Y Pharmlab Co., Ltd.  
Tel: 021-64340559
Email: xinyu_shi@jwypharmlab.com.cn
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: Capot Chemical Co.,Ltd.  
Tel: +86-(0)57185586718 +86-13336195806
Email: sales@capot.com

1-Methylcyclopropanecarbohydrazide manufacturers

1-Methylcyclopropanecarbohydrazide Basic information
Product Name:1-Methylcyclopropanecarbohydrazide
Synonyms:1-METHYLCYCLOPROPANECARBOXYLIC ACID HYDRAZIDE;1-methylcyclopropane-1-carbohydrazide;1-Methylcyclopropanecarbohydrazide
CAS:72790-89-7
MF:C5H10N2O
MW:114.15
EINECS:
Product Categories:
Mol File:72790-89-7.mol
1-Methylcyclopropanecarbohydrazide Structure
1-Methylcyclopropanecarbohydrazide Chemical Properties
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
pka13.46±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
1-Methylcyclopropanecarbohydrazide Usage And Synthesis
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
1-Methylcyclopropanecarbohydrazide Preparation Products And Raw materials
Raw materialsEthyl 1-methylcyclopropane-1-carboxylate-->Hydrazine hydrate-->Toluene
Tag:1-Methylcyclopropanecarbohydrazide(72790-89-7) Related Product Information
1-Methylcyclopropanecarbohydrazide 2-methylcyclopropanecarbohydrazide 2,2-dichloro-N'-[(1,5-dimethyl-1H-pyrazol-4-yl)methylene]-1-methylcyclopropanecarbohydrazide 2,2-dibromo-N'-[(5-{2-chloro-5-nitrophenyl}-2-furyl)methylene]-1-methylcyclopropanecarbohydrazide 2,2-dichloro-N'-[(1-ethyl-3-methyl-1H-pyrazol-4-yl)methylene]-1-methylcyclopropanecarbohydrazide 2,2-dibromo-N'-[(5-bromo-2-thienyl)methylene]-1-methylcyclopropanecarbohydrazide 2,2-dibromo-N'-[1-(4-ethoxyphenyl)propylidene]-1-methylcyclopropanecarbohydrazide 2,2-dibromo-N'-({5-[(3,4-dichlorophenoxy)methyl]-2-furyl}methylene)-1-methylcyclopropanecarbohydrazide 2,2-dibromo-N'-{3-[(4-cyanophenoxy)methyl]-4-methoxybenzylidene}-1-methylcyclopropanecarbohydrazide 2,2-dibromo-N'-[1-(4-butoxyphenyl)propylidene]-1-methylcyclopropanecarbohydrazide 1-Methylcyclopropane-1,2-dicarbohydrazide hydrate N'-(1,3-benzodioxol-5-ylmethylene)-2,2-dibromo-1-methylcyclopropanecarbohydrazide RARECHEM AQ NN 0336 RARECHEM AQ C3 0031 2,2-Dibromo-1-methyl-cyclopropanecarboxylic acid hydrazide 2,2-Dichloro-1-methylcyclopropanecarbohydrazide 2-Bromo-1-methyl-cyclopropanecarboxylic acid hydrazide 2,2-Dibromo-1-methylcyclopropanecarbohydrazide