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2-Cyclopropene-1-carboxaldehyde, 2,3-diphenyl- is a chemical compound with the molecular formula C17H12O. It is a derivative of cyclopropene-1-carboxaldehyde, featuring two phenyl groups attached to the cyclopropane ring. This molecule is characterized by its unique structure, which includes a three-membered carbon ring (cyclopropane) and an aldehyde functional group. It is an organic compound that can be used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its reactive nature and the presence of the phenyl groups, which can participate in various chemical reactions. The compound is typically handled with care due to its potential reactivity and should be stored and used according to proper safety protocols.

3763-36-8

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3763-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3763-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3763-36:
(6*3)+(5*7)+(4*6)+(3*3)+(2*3)+(1*6)=98
98 % 10 = 8
So 3763-36-8 is a valid CAS Registry Number.

3763-36-8Relevant academic research and scientific papers

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

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, (2019/10/29)

An organic light emitting device (OLED) that includes an anode, a cathode, and an organic layer disposed between the anode and the cathode. The organic layer includes a metal compound that comprises a ligand LA of Formula I, wherein the dashed

Gold(I)-catalyzed cycloisomerization of enynes containing cyclopropenes

Li, Changkun,Zeng, Yi,Zhang, Hang,Feng, Jiajie,Zhang, Yan,Wang, Jianbo

supporting information; experimental part, p. 6413 - 6417 (2010/11/19)

Goldenyne: Gold-catalyzed cycloisomerization reactions of propargyl cyclopropenes afford benzene derivatives in a highly efficient manner. The reaction either proceeds through a mechanism with or without double and triple bond cleavage, depending on the substituents (see scheme). Copyright

Small Rings, 33. Attempts to Synthesize Diphenyltetrahedrane

White, Emil H.,Winter, Rudolph E. K.,Graeve, Rolf,Zirngibl, Ulrich,Friend, Earl W.,et al.

, p. 3906 - 3915 (2007/10/02)

Carbene 7, formed on photochemical or thermal excitation of (2,3-diphenyl-2-cyclopropen-1-yl)diazomethane (6i), splits mostly into two acetylenes 8 and 9 instead of undergoing an intramolecular cycloaddition.Photolysis of the Masamune ketone 16 depending on the reaction conditions gives either p-terphenyl or a mixture of the two cyclooctatetraens 18 and 19.The intermediate formation of tetrahedrane 10 would fit into the mechanistic picture of this fragmentation.

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