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The chemical compound "(3aR,10bS,11S,12bS)-5-Methyl-1-oxo-11-phenylsulfanyl-3a,11,12,12b-tetrahydro-1H,4H-6,12a-diaza-indeno[7,1-cd]fluorene-6-carboxylic acid methyl ester" is a complex organic molecule with a unique structure. It features a methyl group at the 5th position, a carbonyl group at the 1st position, and a phenylsulfanyl group at the 11th position. The compound is characterized by its tetrahydro-1H,4H-6,12a-diaza-indeno[7,1-cd]fluorene core, which is a fused ring system with nitrogen atoms at the 6 and 12a positions. The molecule also includes a 6-carboxylic acid group that is esterified with a methyl group, indicating the presence of a methyl ester. (3aR,10bS,11S,12bS)-5-Methyl-1-oxo-11-phenylsulfanyl-3a,11,12,12b-tetrahydro-1H,4H-6,12a-diaza-indeno[7,1-cd]fluorene-6-carboxylic acid methyl ester's specific stereochemistry is defined by the (3aR,10bS,11S,12bS) configuration, which describes the three-dimensional arrangement of atoms around the chiral centers. The compound's complexity and unique structure suggest potential applications in various fields, such as pharmaceuticals or materials science, where its specific properties could be harnessed for specific functions.

98359-07-0

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98359-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98359-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,5 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98359-07:
(7*9)+(6*8)+(5*3)+(4*5)+(3*9)+(2*0)+(1*7)=180
180 % 10 = 0
So 98359-07-0 is a valid CAS Registry Number.

98359-07-0Downstream Products

98359-07-0Relevant academic research and scientific papers

METHODS FOR INDOLE ALKALOID SYNTHESIS. A HIGHLY CONVERGENT STRATEGY FOR THE SYNTHESIS OF A 3-METHYL-6,7-DEHYDROASPIDOSPERMIDINE SYSTEM.

Magnus, Philip,Cairns, Peter M.,Kim, Chung Sook

, p. 1963 - 1966 (2007/10/02)

The N1-CO2Me derivative of 2-ethyl-3-formylindole has been converted into the highly functionalized aspidospermidine-type alkaloid 12 in four steps.

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