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The chemical compound in question is a complex organic molecule with the formula (10S)-3c-(4-nitro-benzoyloxy)-10r.13c-dimethyl-17c-((R)-1.5-dimethyl-hexyl)-(5tH.8cH.9tH.14tH)-hexadecahydro-1H-cyclopenta[a]phenanthrene. (10S)-3c-(4-nitro-benzoyloxy)-10r.13c-dimethyl-17c-((R)-1.5-dimethyl-hexyl)-(5tH.8cH.9tH.14tH)-hexadecahydro-1H-cyclopenta[a]phenanthrene features a cyclopenta[a]phenanthrene core, which is a type of polycyclic aromatic hydrocarbon. It has a 4-nitro-benzoyloxy group attached to the 3c position, a dimethyl group at the 10r and 13c positions, and a chiral (R)-1.5-dimethyl-hexyl group at the 17c position. The compound also has a hexadecahydro structure, indicating the presence of sixteen hydrogen atoms in a cyclic structure, and a 1H-cyclopenta[a]phenanthrene ring system, which contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

35599-21-4

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35599-21-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35599-21-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,9 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35599-21:
(7*3)+(6*5)+(5*5)+(4*9)+(3*9)+(2*2)+(1*1)=144
144 % 10 = 4
So 35599-21-4 is a valid CAS Registry Number.

35599-21-4Downstream Products

35599-21-4Relevant academic research and scientific papers

Mitsunobu-like Processes with a Novel Triphenylphosphine-Cyclic Sulfamide Betaine

Castro, Jose L.,Matassa, Victor G.,Ball, Richard G.

, p. 2289 - 2291 (1994)

An unprecedented adduct 10 between triphenylphosphine (TPP) and 3,3-dimethyl-1,2,5-thiadiazolidine 1,1-dioxide (8) is described, which can be regarded as a stable source of the (1+) species, and was utilized to efficiently promote the coupling betwe

Efficacious modification of the Mitsunobu reaction for inversions of sterically hindered secondary alcohols

Martin,Dodge

, p. 3017 - 3020 (2007/10/02)

A practical modification of the Mitsunobu protocol for effecting stereochemical inversions of alcohols has been discovered in which use of p-nitrobenzoic acid as the nucleophilic partner results in significantly improved yields with relatively hindered su

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