95713-50-1

Basic information

• Product Name: Cyclopropanecarboxylic acid, 1-cyano-2,2-dimethyl-3-phenyl-, ethyl ester
• CAS NO: 95713-50-1
• Molecular Formula: C15H17NO2
• Molecular Weight: 243.305
• Mol File: 95713-50-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclopropanecarboxylic acid, 1-cyano-2,2-dimethyl-3-phenyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopropanecarboxylic acid, 1-cyano-2,2-dimethyl-3-phenyl-, ethyl ester(95713-50-1)
• EPA Substance Registry System: Cyclopropanecarboxylic acid, 1-cyano-2,2-dimethyl-3-phenyl-, ethyl ester(95713-50-1)

Safety Data

• Hazardous Substances Data: 95713-50-1(Hazardous Substances Data)

Upstream product

• 79-46-9 2-nitropropane 
• 2169-69-9 ethyl (E)-2-cyano-3-phenyl-2-propenoate 
• 100-52-7 benzaldehyde 
• 105-56-6 ethyl 2-cyanoacetate 
• 2025-40-3 ethyl benzylidenecyanoacetate 
• 6731-58-4 ethyl 2-cyano-3-phenylpropanoate 

Downstream Products

• 99647-67-3 cis-2,2-dimethyl-3-phenylcyclopropane-1-carbonitrile 
• 99647-67-3 (+/-)-trans-2,2-dimethyl-3-phenylcyclopropanecarbonitrile 
• 103012-03-9 (1R,3S)-1-Cyano-2,2-dimethyl-3-phenyl-cyclopropanecarboxylic acid 

Relevant articles and documents

Direct Cyclopropanation of α-Cyano β-Aryl Alkanes by Light-Mediated Single Electron Transfer Between Donor–Acceptor Pairs

Cyclopropanes are traditionally prepared by the formal [2+1] addition of carbene or radical based C1 units to alkenes. In contrast, the one-pot intermolecular cyclopropanation of alkanes by redox active C1 units has remained unrealised. Herein, we achieve

Cyclopropyl aryl amide derivatives and uses thereof

Compounds of the formula: wherein Ar1, Ar2, R1 and R2 are as defined herein. Also provided are pharmaceutical compositions, methods of using, and methods of preparing the subject compounds.

A TANDEM MICHAEL REACTION-CYCLOALKYLATION UTILIZING 2-NITROPROPANE: A FACILE ROUTE TO THE ACID COMPONENT OF INSECTICIDAL PYRETHROIDS

Treatment of three representative β-substituted-α-cyanoacrylates (2) with 2-nitropropane and potassium carbonate in refluxing ethanol afforded stereoselectively cyclopropanoid precursors (4) to 3-substituted-2,2-dimethylcyclopropanecarboxylic acids (7).