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(3aR,4R,7aR)-4-[2-(3-Methoxy-phenyl)-ethyl]-7a-methyl-1-methylene-octahydro-inden-5-one is a complex organic compound with a unique molecular structure. It is characterized by its octahydro-inden-5-one core, which is a type of cyclic ketone. The compound features a 3-methoxy-phenylethyl group attached to the 4-position, providing a methoxy substituent on the phenyl ring. Additionally, it has a methyl group at the 7a-position and a methylene group at the 1-position, which contributes to its overall structure and potential reactivity. 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.

98006-20-3

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98006-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98006-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98006-20:
(7*9)+(6*8)+(5*0)+(4*0)+(3*6)+(2*2)+(1*0)=133
133 % 10 = 3
So 98006-20-3 is a valid CAS Registry Number.

98006-20-3Relevant academic research and scientific papers

ENANTIOSPECIFIC SYNTHESIS OF ESTRONE

Hutchinson, John H.,Money, Thomas

, p. 1 - 6 (2007/10/02)

Efiicient cleavage of the C(1)-C(2) bond in 9,10-dibromocamphor (3) provides a chiral intermediate (5) that can be used in a new enantiospecific synthesis of estrone.

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