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2,2,4,4-Tetraphenylbutenol-3 is an organic compound characterized by its molecular formula C34H28O. It is a derivative of butenol, featuring a butane-3-ol structure with four phenyl groups attached to the carbon atoms at positions 2, 2, 4, and 4. 2,2,4,4-Tetraphenylbutenol-3 is known for its unique chemical properties, which arise from the presence of the phenyl groups that confer stability and influence its reactivity. It is typically synthesized through various organic reactions and is used in research and development, particularly in the field of organic chemistry, to study the effects of steric hindrance and electronic interactions in molecular structures. The compound's applications may also extend to the synthesis of more complex molecules and materials, highlighting its importance in advanced chemical research.

41326-73-2

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41326-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41326-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,2 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41326-73:
(7*4)+(6*1)+(5*3)+(4*2)+(3*6)+(2*7)+(1*3)=92
92 % 10 = 2
So 41326-73-2 is a valid CAS Registry Number.

41326-73-2Relevant academic research and scientific papers

CUMULENE PHOTOCHEMISTRY: PHOTOADDITION OF NEUTRAL METHANOL TO PHENYLALLENES

Klett, Michael W.,Johnson, Richard P.

, p. 1107 - 1110 (2007/10/02)

Ultraviolet irradiation of tetra-, tri-, or diphenylallene in methanol leads to allylic methyl ethers. A mechanism is proposed with intermediacy of a strongly polarized planar allene excited state, initially protonated at C2.

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