6228-73-5

Basic information

• Product Name: CYCLOPROPANECARBOXAMIDE
• Synonyms: TIMTEC-BB SBB008326;CYCLOPROPANECARBOXAMIDE;CYCLOPROPYL CARBOXYAMIDE;CYCLOPROPYLCARBOXAMIDE;Arcado;Seed One;trans-2,2-dichloro-N-(1-(4-chlorophenyl)ethyl)-1-ethyl-3-methylcyclopropanecarboxamide;Win
• CAS NO: 6228-73-5
• Molecular Formula: C₄H₇NO
• Molecular Weight: 85.1
• EINECS: 228-332-3
• Product Categories: Cyclopropanes;Simple 3-Membered Ring Compounds;Fine Chemical
• Mol File: 6228-73-5.mol
• Article Data: 19

Chemical Properties

• Melting Point: 120-122°C
• Boiling Point: 248.5 °C at 760 mmHg
• Flash Point: 104.1 °C
• Appearance: light brown crystalline powder
• Density: 1.187 g/cm³
• Vapor Pressure: 0.0242mmHg at 25°C
• Refractive Index: 1.524
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 16.60±0.20(Predicted)
• Water Solubility: Insoluble in water.
• BRN: 1924346
• CAS DataBase Reference: CYCLOPROPANECARBOXAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOPROPANECARBOXAMIDE(6228-73-5)
• EPA Substance Registry System: CYCLOPROPANECARBOXAMIDE(6228-73-5)

Safety Data

• Hazard Codes: Xi
• Safety Statements: 22-24/25
• TSCA: Yes
• Hazardous Substances Data: 6228-73-5(Hazardous Substances Data)

Usage

Description

Cyclopropanecarboxamide is an organic compound with the chemical structure featuring a cyclopropane ring and a carboxamide group. It is a synthetic molecule that can be utilized in various chemical reactions and processes due to its unique structural properties.

Uses

Used in Chemical Synthesis:
Cyclopropanecarboxamide is used as an intermediate in the synthesis of 2-(cyclopropanecarbonyl-amino)-but-2-enoic acid. This application is based on its reactivity with 2-oxo-butyric acid, which allows for the formation of the desired product through a chemical reaction. The use of Cyclopropanecarboxamide in this context highlights its utility in organic chemistry and the potential for further development of related compounds with specific applications in various industries.

InChI:InChI=1/C4H7NO/c5-4(6)3-1-2-3/h3H,1-2H2,(H2,5,6)

Upstream product

• 4023-34-1 cyclopropanecarboxylic acid chloride 
• 5500-21-0 cyclopropropanecarbonitrile 
• 765-43-5 Cyclopropyl methyl ketone 
• 1759-53-1 cyclopropanecarboxylic acid 
• 99912-18-2 2,3,4,5,-Tetrahydro-11-phenyl-1H-[1,4]diazepino[1,7-a]indole 
• 64969-79-5 cyclopropanecarboxylic acid isobutyl ester 
• 63190-44-3 cyclopropanecarboximidic Acid Ethyl Ester Hydrochloride 
• 628-20-6 4-Chlorobutyronitrile 
• 141-52-6 sodium ethanolate 

Downstream Products

• 10528-56-0 bis-cyclopropanecarbonyl-amine 
• 73330-91-3 Methyl N-cyclopropylcarbamate 
• 5500-21-0 cyclopropropanecarbonitrile 
• 765-30-0 Cyclopropylamine 
• 14372-14-6 N-(3-methoxyphenyl)cyclopropanecarboxamide 
• 1170069-87-0 C₁₇H₁₅N₅O 
• 1170069-81-4 C₁₅H₁₂ClN₅O 
• 1239891-65-6 C₁₆H₁₂N₆O 
• 1239891-63-4 C₁₅H₁₃N₅O 
• 1239891-81-6 C₁₆H₁₄FN₅O 
• 1258295-31-6 2,6-dichloro-N-(2-(cyclopropanecarboxamido)pyridin-4-yl)-4-(1H-pyrazol-4-yl)benzamide 
• 1258295-16-7 2,6-dichloro-N-(2-(cyclopropanecarboxamido)pyridin-4-yl)-4-ethynylbenzamide 
• 1258294-32-4 2,6-dichloro-N₁-(2-(cyclopropanecarboxamido)pyridin-4-yl)-N₄,N₄-dimethylterephthalamide 
• 1438897-20-1 2,6-dichloro-N-(2-(cyclopropanecarboxamido)pyridin-4-yl)-4-(3-hydroxyprop-1-yn-1-yl)benzamide 

Relevant articles and documents

Novel method and technology for synthesizing cyclopropyl ammonia

The invention discloses a synthesis process route of a cyclopropane synthetic route. In the process route, cyanocyclopropane 1 - formic acid (-1 -) and (1) are subjected to hydrolysis under the action of a strong base to generate 1-cyanocyclopropane 1 - formic acid (-1 -), (2) decarboxylation to generate cyclopropanecarboxamide (2 3), and (4 4 3) subjected to Hoffman rearrangement to obtain the target product cyclopropysite. The process route is longer than the production process in the present stage, the reaction route is long, the use of high-temperature and high-pressure is avoided, the danger is reduced, and the safety is improved. The requirement of the reaction equipment is reduced, the used raw materials are easy to obtain, operation is easy, safety and environmental protection are achieved, and industrial production can be realized.

Efficient Hydration of Nitriles Promoted by Gallic Acid Derived from Renewable Bioresources

An efficient gallic acid promoted nitriles hydration at room temperature with ethanol/water as a solvent has been developed. The present protocol offers a wide range of amides in moderate to good yields. Moreover, galla chinensis extract can serve as the promoter to perform the hydration, which also shows the potential utilization of natural feedstocks.

Corresponding amine nitrile and method of manufacturing thereof

The invention relates to a manufacturing method of nitrile. Compared with the prior art, the manufacturing method has the characteristics of significantly reduced using amount of an ammonia source, low environmental pressure, low energy consumption, low production cost, high purity and yield of a nitrile product and the like, and nitrile with a more complex structure can be obtained. The invention also relates to a method for manufacturing corresponding amine from nitrile.