37555-48-9

Basic information

• Product Name: (2,2-diphenylcyclopropyl)Methanol
• Synonyms: (2,2-diphenylcyclopropyl)Methanol
• CAS NO: 37555-48-9
• Molecular Formula: C₁₆H₁₆O
• Molecular Weight: 224.3
• Mol File: 37555-48-9.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2,2-diphenylcyclopropyl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2,2-diphenylcyclopropyl)Methanol(37555-48-9)
• EPA Substance Registry System: (2,2-diphenylcyclopropyl)Methanol(37555-48-9)

Safety Data

• Hazardous Substances Data: 37555-48-9(Hazardous Substances Data)

Usage

Description

(2,2-diphenylcyclopropyl)Methanol is a chemical compound with the molecular formula C15H14O. It is a cyclopropyl derivative that contains two phenyl groups attached to the cyclopropyl ring. (2,2-diphenylcyclopropyl)Methanol is known for its unique structural and chemical properties, making it a valuable asset in the fields of organic synthesis and pharmaceutical research.

Uses

Used in Organic Synthesis:
(2,2-diphenylcyclopropyl)Methanol is used as a building block for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse properties and applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2,2-diphenylcyclopropyl)Methanol serves as a key intermediate in the development of new drugs. Its cyclopropyl-containing structure is of particular interest, as it can contribute to the biological activity of the resulting pharmaceuticals.
Used in the Study of Cyclopropyl-Containing Molecules:
(2,2-diphenylcyclopropyl)Methanol is also a valuable tool for researchers studying the properties and potential applications of cyclopropyl-containing molecules. Its presence in these molecules can influence their biological activities, making it an important compound for understanding the role of cyclopropyl groups in drug discovery and development.

Upstream product

• 19481-83-5 1-bromo-2,2-diphenylcyclopropanecarboxylic acid 
• 119-61-9 benzophenone 
• 59591-01-4 2,2-diphenylcyclopropanecarbaldehyde 
• 677-22-5 tert-butylmagnesium chloride 
• 25152-47-0 2,2-diphenyl-1-methylenecyclopropane 
• 908093-98-1 diazodiphenylmethane 
• 5350-57-2 benzophenone hydrazone 
• 530-48-3 1,1-Diphenylethylene 
• 19179-60-3 methyl 2,2-diphenylcyclopropane-1-carboxylate 
• 67428-04-0 ethyl 2,2-diphenylcyclopropane-1-carboxylate 
• 439599-07-2 [(2,2-diphenylcyclopropyl)methyl]trichlorosilane 
• 7150-12-1 2,2-diphenyl-cyclopropanecarboxylic acid 
• 107-18-6 allyl alcohol 

Downstream Products

• 50324-00-0 <2,2-Diphenyl-cyclopropyl-(1)>-methyl-p-toluolsulfonat 
• 1449327-81-4 7-hydroxy-1-(2,2-diphenylcyclopropyl)-5,5-bis(phenylsulfonyl)hept-2-yn-1-one 
• 1449327-63-2 dimethyl 2-[2-(tert-butyldimethylsilyloxy)ethyl]-2-[4-(2,2-diphenylcyclopropyl)-4-oxobut-2-ynyl]malonate 
• 1449327-56-3 1-acetoxy-1-(2,2-diphenylcyclopropyl)hex-2-yn-6-ol 
• 1449327-58-5 1-methoxy-1-(2,2-diphenylcyclopropyl)hex-2-yn-6-ol 
• 1449327-59-6 6-hydroxy-1-(2,2-diphenylcyclopropyl)hex-2-yn-1-one 
• 1449327-61-0 7-hydroxy-1-(2,2-diphenylcyclopropyl)hept-2-yn-1-one 
• 1449327-74-5 6-hydroxy-5,5-dimethyl-1-(2,2-diphenylcyclopropyl)hex-2-yn-1-one 
• 1449327-79-0 N-[4-(2,2-diphenylcyclopropyl)-4-oxobut-2-ynyl]-N-(2-hydroxyethyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Platinum complex-catalyzed hydrosilylation of 2,2-diaryl-1-methylenecyclopropane affording (silylmethyl)cyclopropane

PtI2(PPh3)2-catalyzed hydrosilylation of 2,2-diphenyl-1-methylenecyclopropane with HSiEt3 forms (2,2-diphenylcyclopropyl)methyl(triethyl)silane in 87% yield as a sole product. This highly selective addition of S

Evidence that Additions of Grignard Reagents to Aliphatic Aldehydes Do Not Involve Single-Electron-Transfer Processes

Addition of allylmagnesium reagents to an aliphatic aldehyde bearing a radical clock gave only addition products and no evidence of ring-opened products that would suggest single-electron-transfer reactions. The analogous Barbier reaction also did not pro

Aryl-substituted cyclopropyl acetylenes as sensitive mechanistic probes in the gold-catalyzed hydration of alkynes. comparison to the Ag(I)-, Hg(II)-, and Fe(III)-catalyzed processes

The gold-catalyzed hydration of 2-phenyl- or 2,2-diphenylcyclopropyl acetylene, sensitive probes to trace the formation of vinyl carbocations, provides exclusively the corresponding cyclopropyl methyl ketones. On the other hand, in the Ag(I)- or Fe(III)-c

Concerning the reactivity of ptad with isomeric dienes: The mechanism of the Diels-Alder cycloaddition

Cyclopropyl substituted dienes are employed as mechanistic probes in the triazolinedione Diels-Alder (DA) reaction. In aprotic and protic solvents, apart from the DA adducts that bear an intact cyclopropyl group, complicated and rearranged products are also obtained. These results provide solid evidence for the involvement of an open intermediate with a lifetime greater than 2 x 10 -12 s.