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1,2-Diphenyl-3-hydroxymethyl-1-cyclopropene is a complex organic compound characterized by a cyclopropene ring, which is a three-carbon cyclic structure with a double bond, and two phenyl groups attached to the first and second carbon atoms. The third carbon atom in the cyclopropene ring is bonded to a hydroxymethyl group, which consists of a hydroxyl group (-OH) and a methyl group (-CH3). This molecule is known for its unique structure and potential applications in organic synthesis, particularly in the formation of complex molecular architectures. It is also of interest in the study of strained ring systems due to the high degree of ring strain inherent in the cyclopropene motif. The compound's properties, such as reactivity and stability, are influenced by the presence of the phenyl groups and the hydroxymethyl substituent, making it a subject of interest in chemical research and development.

6415-73-2

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6415-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6415-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6415-73:
(6*6)+(5*4)+(4*1)+(3*5)+(2*7)+(1*3)=92
92 % 10 = 2
So 6415-73-2 is a valid CAS Registry Number.

6415-73-2Relevant academic research and scientific papers

Cu(I)-Catalyzed Intramolecular Tandem Cyclization of N-Indole-Tethered Cyclopropenes: Synthesis of Functionalized Hydrogenated Diazabenzo[ a]cyclopenta[ cd]azulene Derivatives

Li, Peng-Hua,Yang, Song,Hao, Tong-Gang,Xu, Qin,Shi, Min

, (2019/05/07)

A Cu(I)-catalyzed [3 + 2] intramolecular cycloaddition reaction of N-indole-tethered cyclopropenes is presented in this paper. This reaction starts from the formation of ?-allyl cationic intermediate or its resonance-stabilized metal carbenoid intermediate upon activation of cyclopropene with Cu(I) catalyst and a Friedel-Crafts-type cyclization to give functionalized hydrogenated diazabenzo[a]cyclopenta[cd]azulenes in good to excellent yields along with moderate to good dr values. The asymmetric variant of this cycloaddition reaction can be realized, giving the desired products with moderate ee values.

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

RhI-Catalyzed Carbonylative [3+1] Construction of Cyclobutenones via C?C σ-Bond Activation of Cyclopropenes

Xu, Wen-Bin,Li, Changkun,Wang, Jianbo

, p. 15786 - 15790 (2018/10/15)

With a catalytic amount of Rh(cod)2BF4 and dppm, cyclopropenes undergo a direct carbonylative [3+1] cycloaddition reaction under an atmosphere of CO to produce the cyclobutenones in excellent yields, in which the regio- and diastereoselectivities can be controlled in certain cases with the help of chelating groups. Cyclobutenone with a chiral 4-position was prepared by diastereoselective induction. Rhodacyclopentenone has been determined as the key intermediate, as it was synthesized and applied to the reductive elimination step.

The Attempted Generation of a Methylene-Bridged Trimethylenemethane Biradical (1,3-Diphenyl-2-methylenecyclobutane-1,3-diyl) by Oxidation of endo-1,3-Diphenyl-2-(phenylselenomethyl)bicyclobutane.

Bushby, Richard J.,Jesudason, Malini V.

, p. 1144 - 1170 (2007/10/02)

Copper-catalysed addition of ethyl diazoacetate to diphenylacetylene and hydrolysis gives 1,2-diphenylcyclopropane-3-carboxylic acid (18b).Conversion to the acid chloride (18c) and reduction with lithium aluminium tri-tert-butoxy hydride gives 1,2-dipheny

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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