Spironolactone Related Compound C

CAS: 976-70-5

Ref. 3D-AAA97670

Product Information

• Name: Spironolactone Related Compound C
• Synonyms: (8R,9S,10R,13S,14S,17R)-10,13-dimethyl-1,6,7,8,9,10,11,12,13,14,15,16-dodecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-3,5'(2H,4'H)-dione, 17-alpha-Pregn-4-ene-21-carboxylic acid, 17-hydroxy-3-oxo-, gamma-lactone, 17α-Pregn-4-ene-21-carboxylic acid, 17-hydroxy-3-oxo-, γ-lactone, 17β-Hydroxy-3-oxopregn-4-en-21-carboxylic acid γ-lactone, 20-Spirox-4-ene-3,20-dione, 3-(3-Oxo-17-beta-hydroxy-4-androsten-17-alpha-yl)propionic acid gamma-lactone, 3-(3-Oxo-17β-hydroxy-4-androsten-17-yl)propionic acid γ-lactone, 3-(3-Oxo-17β-hydroxyandrost-4-en-17α-yl)propiolactone, 3-Oxopregn-4-ene-21,17alpha-carbolactone, 3′-(3-Oxo-17β-hydroxyandrost-4-en-17α-yl)-propionic acid lactone, 6,7-Dihydrocanrenone, Brn 0043765, Pregn-4-ene-21-carboxylic acid, 17-hydroxy-3-oxo-, γ-lactone, (17α)-, Sc 5233, Spirolactone, omega-(3-Oxo-17-beta-hydroxy-4-androsten-17-alpha-yl) propionic acid lactone

Description

Spironolactone Related Compound C is a chiral molecule that has been synthesized by the ring-opening of an asymmetric meso-diamine. The product was obtained in high yield, with a transition temperature of -35°C and plates that are oriented on the surface. This compound has been shown to be activated by paraformaldehyde and low yield, as well as oriented into a chiral form. It can be thermally multistep to produce other compounds such as spironolactone and its derivatives. Spironolactone Related Compound C is also irreversibly oxidized by sulfur in the presence of catalysts such as copper sulfate and potassium dichromate.

• Brand: Biosynth

Chemical properties

• Molecular weight: 342.47 g/mol
• Formula: C₂₂H₃₀O₃
• Purity: Min. 95%