139633-98-0

Basic information

• Product Name: (1-ETHYNYLCYCLOPROPYL)BENZENE
• Synonyms: (1-ETHYNYLCYCLOPROPYL)BENZENE;1-phenyl-1-ethynylcyclopropane;Benzene, (1-ethynylcyclopropyl)-;1-(1-ethynylcyclopropyl)benzene;(1-Ethynylcyclopropyl)
• CAS NO: 139633-98-0
• Molecular Formula: C₁₁H₁₀
• Molecular Weight: 142.2
• EINECS: 604-604-1
• Mol File: 139633-98-0.mol

Chemical Properties

• Boiling Point: 199.1°C at 760 mmHg
• Flash Point: 62.7°C
• Appearance: /
• Density: 1.02g/cm³
• Vapor Pressure: 0.491mmHg at 25°C
• Refractive Index: 1.572
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (1-ETHYNYLCYCLOPROPYL)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: (1-ETHYNYLCYCLOPROPYL)BENZENE(139633-98-0)
• EPA Substance Registry System: (1-ETHYNYLCYCLOPROPYL)BENZENE(139633-98-0)

Safety Data

• Hazardous Substances Data: 139633-98-0(Hazardous Substances Data)

Usage

Uses

As the provided materials do not specify the uses of (1-Ethynylcyclopropyl)benzene, it is not possible to list its applications based on the given information. Further research and investigation would be required to determine its potential uses in various industries or applications.

InChI:InChI=1/C11H10/c1-2-11(8-9-11)10-6-4-3-5-7-10/h1,3-7H,8-9H2

Upstream product

• 28557-00-8 phenylzinc chloride 
• 38387-33-6 1-chloro-1-ethynylcyclopropane 
• 6120-95-2 1-phenyl-1-cyclopropane carboxylic acid 
• 21744-88-7 1-phenylcyclopropanecarbaldehyde 
• 27491-70-9 dimethyl diazomethylphosphonate 
• 935-44-4 1-cyano-1-phenylcyclopropane 

Relevant articles and documents

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Nucleophilic substitutions of 1-alkenylcyclopropyl esters and 1-alkynylcyclopropyl chlorides catalyzed by palladium(0)

The 1-ethenylcyclopropylsulfonates 2e,f and 2-cyclopropylideneethyl esters 10b,c, readily available from cyclopropanone hemiacetal 1, undergo regioselective Pd(0) catalyzed nucleophilic substitution via the unsymmetric 1,1-dimethylene-π-allyl complex 23. With stabilized anions (enolates of malonic ester, β-dicarbonyl compounds, β-sulfonyl ester, and Schiff bases as well as acetate anion, sulfonamide anion, etc.) the nucleophilic substitution occurs at the terminal vinylic position exclusively, providing cyclopropylideneethyl derivatives as building blocks of high synthetic potential. Competition experiments have disclosed that 1-ethenylcyclopropyl tosylate (2e) and cyclopropylideneethyl acetate (10b) are more reactive than dimethylallyl acetates 19 and 22, respectively. Use of chiral phosphines as ligands in the palladium catalyst can provide optically active methylenecyclopropane derivatives. With phenyl-, methyl-, and even n-butylzinc chloride as nucleophiles, the reaction apparently proceeds with initial transfer of the organic residue to palladium, followed by reductive elimination entailing tertiary substitution on the cyclopropane ring exclusively; the same type of product is obtained with azide and bis(trimethylsilyl)amide. But the site of hydride attack to yield reduction products depends on the hydride source. 1-Alkynylcyclopropyl chlorides 12, 13, and 14 react only with organozinc chlorides (nonstabilized nucleophiles) to provide mixtures of ethenylidenecyclopropanes 65 and alkynylcyclopropanes 66, via the σ-palladium complexes 69 and 70, while chloride 15 undergoes mainly reduction. Other transition metal catalysts (Ni, Mo) also induce substitutions, but with poorer regioselectivity.