30835-61-1

Usage

Classification

Synthetic steroid; derivative of estrone.

Applications

Pharmaceutical research; potential anti-inflammatory and anti-cancer properties.

Effects

Hormone regulation; reproductive health.

Versatility

Wide range of potential applications in the medical and scientific fields.

InChI:InChI=1/C19H16O2/c1-11-9-12-5-3-4-6-13(12)19-17(21-2)10-15-14(18(11)19)7-8-16(15)20/h3-6,9-10H,7-8H2,1-2H3

Upstream product

• 30835-60-0 11-Hydroxy-7-methyl-15,16-dihydro-cyclopenta[a]phenanthren-17-one 
• 77-78-1 dimethyl sulfate 
• 30856-55-4 Acetic acid 7-methyl-17-oxo-16,17-dihydro-15H-cyclopenta[a]phenanthren-11-yl ester 

Relevant academic research and scientific papers

A Kinetic Investigation of the Hydroxide-catalysed Detritiation of Various -15,16-Dihydrocyclopentaphenanthren-17-ones and Related Compounds

The hydroxide-catalysed detritiation rate constants from the C-16 position of a series of substituted -15,16-dihydrocyclopentaphenanthren-17-ones have been measured in a 90:10 (v/v) water-dioxane mixture at 25 deg C.The results show that methyl group substitution brings with it, in addition to the costumary deactivating effect, a marked acceleration in rate, which probably has its origin in steric strain considerations.Similar studies involving the analogous position in a number of related ketones (benzindanone, indanone, and cyclopentanone) show that the rates are not simply a function of the number of additional benzene rings but depend on their position relative to the cyclopentanone system.