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The chemical compound "(5S,10R,13R,17R)-17-((R)-1,5-Dimethyl-hexyl)-3-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-6-one" is a complex organic molecule with a unique structure. It is a stereospecific compound, indicated by the presence of the "R" and "S" prefixes, which denote the specific arrangement of atoms in three-dimensional space. The compound features a cyclopenta[a]phenanthren-6-one core, which is a type of polycyclic aromatic hydrocarbon with a five-membered ring fused to a phenanthrene structure. The molecule also includes a 3-hydroxy group, indicating the presence of a hydroxyl group attached to a carbon atom, and two methyl groups at the 10th and 13th positions, which contribute to its branching. The 17th position is occupied by a long alkyl chain, specifically a (R)-1,5-dimethyl-hexyl group, which adds to the molecule's complexity and potential biological activity. (5S,10R,13R,17R)-17-((R)-1,5-Dimethyl-hexyl)-3-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-6-one is likely to be found in natural products or synthesized for specific applications due to its intricate structure and potential pharmacological properties.

6579-82-4

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6579-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6579-82-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6579-82:
(6*6)+(5*5)+(4*7)+(3*9)+(2*8)+(1*2)=134
134 % 10 = 4
So 6579-82-4 is a valid CAS Registry Number.

6579-82-4Relevant academic research and scientific papers

BRASSINOSTEROIDS WITH A CHOLESTANE SIDE CHAIN

Kohout, Ladislav,Strnad, Miroslav

, p. 447 - 458 (2007/10/02)

The synthesis of 2α,3α-dihydroxy-B-homo-7-oxa-cholestan-6-one (VI), 2β,3β-dihydroxy-B-homo-7-oxa-5α-cholestan-6-one (VIII) and 2α,3α-dihydroxy-B-homo-6-oxa-5α-cholestan-7-one (XI) is described.The activity of these brassinosteroids in the bean second internode bioassay is lower than the activity of 24-epibrassinolide (XXI).

A Novel Method for Preparation of Steroidal Ketoximes from Nitroolefins

Habib, Rubina,Husain, Mubarak,Husain, Mashkoor,Khan, Naseem H.

, p. 801 (2007/10/02)

Steroidal 6-nitroolefins (I-IV) undergo facile reaction with NH3-MeOH-Zn yielding exclusively the corresponding 6-one oximes (V-VIII) in quantitative yields.The method appears to be of general applicability.

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