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(Z)-2-Benzyl-4-phenyl-but-2-en-1-ol is an organic compound with the molecular formula C18H18O. It is a chiral molecule, featuring a double bond between the second and third carbon atoms, which gives it the (Z) configuration. (Z)-2-Benzyl-4-phenyl-but-2-en-1-ol consists of a benzyl group attached to the second carbon and a phenyl group on the fourth carbon, with a hydroxyl group on the first carbon. It is a colorless liquid with a distinct aroma and is used in the synthesis of various pharmaceuticals, fragrances, and other organic compounds. Due to its complex structure, it is often synthesized through multi-step reactions involving the use of catalysts and reagents.

36727-46-5

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36727-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36727-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,2 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36727-46:
(7*3)+(6*6)+(5*7)+(4*2)+(3*7)+(2*4)+(1*6)=135
135 % 10 = 5
So 36727-46-5 is a valid CAS Registry Number.

36727-46-5Downstream Products

36727-46-5Relevant academic research and scientific papers

PALLADIUM-CATALYZED REGIO- AND STEREOSELECTIVE DESULFONYLATION OF ALLYLIC SULFONES WITH LiHBEt3. APPLICATION TO THE SYNTHESIS OF SQUALENE

Mohri, Mitsunobu,Kinoshita, Hideki,Inomata, Katsuhiko,Kotake, Hiroshi

, p. 451 - 454 (1985)

Allylic p-tolyl sulfones were easily desulfonylated to the corresponding alkenes by LiHBEt3 in the presence of a catalytic amount of under mild conditions with the preservation of the original stereochemistry.This reaction was successfully applied to the synthesis of squalene.

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