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(3aR,4R,7aR)-4-[2-(3-Methoxy-phenyl)-ethyl]-7a-methyl-hexahydro-indene-1,5-dione is a complex organic compound with a molecular formula of C18H22O3. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry at the 3a, 4, and 7a positions. The compound features a hexahydro-indene core, which is a type of cycloalkene, and it has a 1,5-dione functional group, indicating the presence of two carbonyl groups at the 1 and 5 positions. Additionally, it has a 3-methoxy-phenylethyl substituent attached to the 4 position, which contributes to its unique structure and potential properties. (3aR,4R,7aR)-4-[2-(3-Methoxy-phenyl)-ethyl]-7a-methyl-hexahydro-indene-1,5-dione may be of interest in various fields, such as pharmaceuticals or materials science, due to its specific structural features and potential applications in the synthesis of more complex molecules.

98049-49-1

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98049-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98049-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,4 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98049-49:
(7*9)+(6*8)+(5*0)+(4*4)+(3*9)+(2*4)+(1*9)=171
171 % 10 = 1
So 98049-49-1 is a valid CAS Registry Number.

98049-49-1Downstream Products

98049-49-1Relevant academic research and scientific papers

An oxidative free-radical cyclization approach to d,l-Δ8-14-epiestrone-3-methyl ether

Zoretic,Ramchandani,Caspar

, p. 923 - 929 (2007/10/02)

A stereospecific free-radical cyclization of β-keto esters 4 and 5 to cis-hydrindanones 9 and 6, respectively, and conversion of 6 to d,l-14-epiestrone intermediate 8 are resported.

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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