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(2,3-Diphenyl-2-cyclopropen-1-yl)diazomethane is a complex organic compound with the molecular formula C17H14N2. It is characterized by a cyclopropenyl ring fused to a diazomethane group, with two phenyl rings attached to the cyclopropane. This molecule is known for its highly reactive nature due to the presence of the diazomethane moiety, which contains a carbon-nitrogen double bond. It is used as a reagent in organic synthesis, particularly for the formation of carbocations and in various cyclopropanation reactions. Due to its instability and potential toxicity, it requires careful handling and is typically generated in situ for immediate use.

5526-09-0

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5526-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5526-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5526-09:
(6*5)+(5*5)+(4*2)+(3*6)+(2*0)+(1*9)=90
90 % 10 = 0
So 5526-09-0 is a valid CAS Registry Number.

5526-09-0Relevant academic research and scientific papers

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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