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1,2-Didehydrocondyfolan is a naturally occurring sesquiterpene compound, characterized by its unique tricyclic structure. It is found in various plants, particularly in the genus Condylocarpon, and is known for its potential biological activities, such as anti-inflammatory and antimicrobial properties. The compound's name reflects its structure, with "1,2-didehydro" indicating the presence of a double bond between carbon atoms 1 and 2, and "condyfolan" referring to its base structure derived from the condylocarpon genus. Research on 1,2-didehydrocondyfolan and its derivatives is ongoing to explore their potential applications in medicine and pharmaceuticals.

3408-40-0

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3408-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3408-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3408-40:
(6*3)+(5*4)+(4*0)+(3*8)+(2*4)+(1*0)=70
70 % 10 = 0
So 3408-40-0 is a valid CAS Registry Number.

3408-40-0Upstream product

3408-40-0Downstream Products

3408-40-0Relevant academic research and scientific papers

TiCl3-Mediated Synthesis of 2,3,3-Trisubstituted Indolenines: Total Synthesis of (+)-1,2-Dehydroaspidospermidine, (+)-Condyfoline, and (?)-Tubifoline

Delayre, Bastien,Piemontesi, Cyril,Wang, Qian,Zhu, Jieping

, p. 13990 - 13997 (2020/06/10)

2,3,3-Trisubstituted indolenine constitutes an integral part of many biologically important monoterpene indole alkaloids. We report herein an unprecedented access to this skeleton by a TiCl3-mediated reductive cyclization of tetrasubstituted alkenes bearing a 2-nitrophenyl substituent. The proof of concept is demonstrated firstly by accomplishing a concise total synthesis of (+)-1,2-dehydroaspidospermidine featuring a late-stage application of this key transformation. A sequence of reduction of nitroarene to nitrosoarene followed by 6π-electron-5-atom electrocyclization and a 1,2-alkyl shift of the resulting nitrone intermediate was proposed to account for the reaction outcome. A subsequent total synthesis of (+)-condyfoline not only illustrates the generality of the reaction, but also provides a mechanistic insight into the nature of the 1,2-alkyl shift. The exclusive formation of (+)-condyfoline indicates that the 1,2-alkyl migration follows a concerted Wagner–Meerwein pathway, rather than a stepwise retro-Mannich/Mannich reaction sequence. Conditions for almost quantitative conversion of (+)-condyfoline to (?)-tubifoline by way of a retro-Mannich/1,3-prototropy/transannular cyclization cascade are also documented.

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