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(1S,4R,5R)-4-Benzyl-2,3-dimethyl-4-phenyl-bicyclo[3.2.0]hept-2-ene is a complex organic compound characterized by its unique bicyclic structure. It features a benzyl group attached to the 4-position, and both 2 and 3 positions are occupied by methyl groups. The phenyl group is also attached to the 4-position, contributing to the molecule's structure. (1S,4R,5R)-4-Benzyl-2,3-dimethyl-4-phenyl-bicyclo[3.2.0]hept-2-ene is a stereoisomer, with the 'S', 'R', and 'R' configurations at the 1st, 4th, and 5th carbon atoms, respectively, which dictate its three-dimensional arrangement. It is a member of the bicyclo[3.2.0]heptene family, indicating a seven-membered ring with two carbon atoms forming a bridge. This specific arrangement of atoms and functional groups gives the compound its distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

74971-45-2

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74971-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74971-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74971-45:
(7*7)+(6*4)+(5*9)+(4*7)+(3*1)+(2*4)+(1*5)=162
162 % 10 = 2
So 74971-45-2 is a valid CAS Registry Number.

74971-45-2Downstream Products

74971-45-2Relevant academic research and scientific papers

Regio- and Stereoselective 1,2 Wagner-Meerwein Shifts during Trifluoroacetic Acid Catalyzed Isomerization of Unsymmetrically Substituted Tricyclo2,4>heptanes

Gree, Rene,Park, Hokoon,Paquette, Leo A.

, p. 4397 - 4403 (2007/10/02)

The regioselectivity and stereoselectivity which materialize upon trifluoroacetic acid promoted isomerization of variously substituted tricyclo2,4>heptanes have been experimentally determined.The highly strained hydrocarbon substrates h

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