158665-23-7

Basic information

• Product Name: Cyclopropanecarboxylic acid, 1-(aminocarbonyl)-2-ethenyl-, cis- (9CI)
• Synonyms: Cyclopropanecarboxylic acid, 1-(aminocarbonyl)-2-ethenyl-, cis- (9CI)
• CAS NO: 158665-23-7
• Molecular Formula: C7H9NO3
• Molecular Weight: 155.15126
• Product Categories: AMIDE;CARBOXYLICACID
• Mol File: 158665-23-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 396.7±42.0 °C(Predicted)
• Appearance: /
• Density: 1.503±0.06 g/cm3(Predicted)
• PKA: 4.04±0.50(Predicted)
• CAS DataBase Reference: Cyclopropanecarboxylic acid, 1-(aminocarbonyl)-2-ethenyl-, cis- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopropanecarboxylic acid, 1-(aminocarbonyl)-2-ethenyl-, cis- (9CI)(158665-23-7)
• EPA Substance Registry System: Cyclopropanecarboxylic acid, 1-(aminocarbonyl)-2-ethenyl-, cis- (9CI)(158665-23-7)

Safety Data

• Hazardous Substances Data: 158665-23-7(Hazardous Substances Data)

Upstream product

• 821-06-7 (E)-1,4-dibromobutene 
• 108-59-8 malonic acid dimethyl ester 
• 17447-60-8 dimethyl 2-vinylcyclopropane-1,1-dicarboxylate 

Relevant articles and documents

OPTICALLY ACTIVE VINYL-CYCLOPROPANE CARBOXYLIC ACID DERIVATIVE AND OPTICALLY ACTIVE VINYL-CYCLOPROPANE AMINO ACID DERIVATIVE MANUFACTURING METHOD

The objective of the present invention is to provide a method for obtaining an optically active vinylcyclopropanecarboxylic acid derivative with high yield and high optical purity using a safe material available at low cost. In addition, the objective of the present invention is to provide a method for safely-obtaining an optically active vinylcyclopropaneamino acid with high optical purity at low cost. The problems can be solved by a method for obtaining an optically active vinylcyclopropanecarboxylic acid derivative, which method contains the step of reacting a racemic vinylcyclopropanecarboxylic acid derivative with an optically active amine compound, to obtain a diastereomer salt of optically active vinylcyclopropanecarboxylic acid derivative - amine compound. In addition, it is possible to obtain a vinylcyclopropaneamino acid by deriving the vinylcyclopropaneamino acid from thus obtained diastereomer salt of optically active vinylcyclopropanecarboxylic acid derivative - amine compound.