24648-07-5

Basic information

• Product Name: Benzene, (2,3,3-trichloro-1-cyclopropen-1-yl)-
• CAS NO: 24648-07-5
• Molecular Formula: C9H5Cl3
• Molecular Weight: 219.498
• Mol File: 24648-07-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, (2,3,3-trichloro-1-cyclopropen-1-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (2,3,3-trichloro-1-cyclopropen-1-yl)-(24648-07-5)
• EPA Substance Registry System: Benzene, (2,3,3-trichloro-1-cyclopropen-1-yl)-(24648-07-5)

Safety Data

• Hazardous Substances Data: 24648-07-5(Hazardous Substances Data)

Upstream product

• 6262-42-6 1,2,3,3-tetrachlorocyclopropene 
• 71-43-2 benzene 

Downstream Products

• 140177-06-6 2-Phenyl-1,3,3-tris(3-methylimidazolium-1-yl)-cyclopropene trichloride 
• 123476-41-5 2-[2-((Z)-2-Hydroxy-2-phenyl-vinyl)-3-phenyl-cycloprop-2-en-(E)-ylidene]-1-phenyl-ethanone 
• 123476-38-0 2-[2-(2-Hydroxy-cyclopent-1-enyl)-3-phenyl-cycloprop-2-en-(Z)-ylidene]-cyclopentanone 
• 123476-42-6 2-(2-Hydroxy-4,4-dimethyl-6-oxo-1-cyclohexenyl)-3-(4,4-dimethyl-2,6-dioxocyclohexanyliden)-1-phenylcyclopropen 
• 61467-21-8 2-Dimethylamino-3-phenylcyclopropenthion 
• 77588-98-8 2-Dimethylamino-3-phenylcyclopropenselenon 
• 123476-37-9 2-[2-(2-Hydroxy-cyclohex-1-enyl)-3-phenyl-cycloprop-2-en-(Z)-ylidene]-cyclohexanone 
• 123476-44-8 3-(2-Hydroxy-1-cyclohexenyl)-2-phenylcyclopropen-1-on 
• 20434-13-3 2-chloro-3-phenylcycloprop-2-en-1-one 
• 1600-39-1 2-hydroxy-3-phenylcyclopropenone 
• 2431-96-1 N,N-diethylphenylacetamide 
• 61077-48-3 2-(diisopropylamino)-3-phenylcycloprop-2-en-1-one 
• 717-78-2 2-(diethylamino)-3-phenylcycloprop-2-en-1-one 

Relevant articles and documents

The Structure and Reactivity of 1,2,3,3-Tetrakis(4-(dimethylamino)pyridinium-1-yl)cyclopropene

The X-ray single crystal structure of 1,2,3,3-tetrakis(4-(dimethylamino)pyridinium-1-yl)cyclopropene, 1, is presented together with some reactions of 1.Both triphenylphosphine and 1-methylimidazole react with 1 to form the ring opened products, (Z)-1-(tri

Phototriggered Dehydration Condensation Using an Aminocyclopropenone

A phototriggered dehydration condensation using an aminocyclopropenone has been developed. The UV irradiation of an aminocyclopropenone generated a highly reactive ynamine in situ and the dehydration condensation of a carboxylic acid and an amine coexisting in the reaction solution smoothly proceeded to afford an amide. This reaction is completely controllable by the ON/OFF states of a UV lamp.

Convenient and General Synthesis of 2-Alkoxy-3-arylcyclopropenones

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