123238-67-5

Basic information

• Product Name: (20R,22S)-2β,3β,14,20,22,25-hexahydro-5β-cholest-7-en-6-one
• Synonyms: (20R,22S)-2β,3β,14,20,22,25-hexahydro-5β-cholest-7-en-6-one
• CAS NO: 123238-67-5
• Molecular Weight: 480.642
• Mol File: 123238-67-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (20R,22S)-2β,3β,14,20,22,25-hexahydro-5β-cholest-7-en-6-one(CAS DataBase Reference)
• NIST Chemistry Reference: (20R,22S)-2β,3β,14,20,22,25-hexahydro-5β-cholest-7-en-6-one(123238-67-5)
• EPA Substance Registry System: (20R,22S)-2β,3β,14,20,22,25-hexahydro-5β-cholest-7-en-6-one(123238-67-5)

Safety Data

• Hazardous Substances Data: 123238-67-5(Hazardous Substances Data)

Upstream product

• 22798-96-5 Crustecdyson-monoacetonid 
• 52717-49-4 26-hydroxyecdysone 
• 3604-87-3 ecdysone 
• 52094-73-2 3-Dehydro-2O-hydroxyecdyson 
• 81655-86-9 sileneoside A 
• 103654-38-2 ecdysterone 22-O-benzoate 
• 135024-06-5 (20R,22R)-22-hydroxy-2β,3β,14,20,25-pentakis-(trimethyl-silanyloxy)-5β-cholest-7-en-6-one 
• 19974-12-0 22-Dehydro-20-hydroxyecdysone 
• 103654-38-2 5α-ecdysterone 22-O-benzoate 
• 131643-66-8 ecdysterone 22,25-di-O-benzoate 

Downstream Products

• 10162-99-9 (2S,3R,5R,10R,13R,14S)-17-Acetyl-2,3,14-trihydroxy-10,13-dimethyl-1,2,3,4,5,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-6-one 
• 103768-04-3 (2S,3R,5R,10R,13R,14S)-17-{(1R,2R)-1,2-Dihydroxy-6-[3-(4-hydroxy-phenyl)-propoxy]-1,5-dimethyl-hexyl}-2,3,14-trihydroxy-10,13-dimethyl-1,2,3,4,5,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-6-one 
• 19536-25-5 20-Hydroxyecdysone-2-acetate 
• 51787-31-6 calonysterone 

Relevant articles and documents

PHYTOECDYSTEROIDS OF PLANTS OF THE GENUS Silene XII. 5α-ECDYSTERONE 22-O-BENZOATE FROM Silene scabrifolia

The new phytoecdysteroid 5α-ecdysterone 22-O-benzoate (I), C34H48O8, mp 262-274 deg C (methanol-water) D20+45.8 deg (methanol), has been isolated from the epigeal organ of Silene scarbiofolia Kom.The alkaline hydrolysis of (I) led to 5α-ecdysterone (II) and benzoic acid.The isomerization of ecdysterone (0.6percent KHCO3 in CH3OH) has yielded (II).Details of the IR, mass, and NMR spectra of compound (I) are given.

A facile route to 20-hydroxyecdysone and side chain homologues from poststeron

A flexible approach to ecdysteroids, chain elongated at C-26 and C-27, is reported. Key features are the addition of 5-lithio 2,3-dihydrofurans (3) to poststeron (10) and a stereoselective reduction of the 22-∞ group.

Seitenkettenhomologe des 20-Hydroxyecdysons: Synthese, Konfigurationsbestimmung und biochemische Charakterisierung

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