178379-35-6

Basic information

• Product Name: (1S,3aS,5S,7aR)-3a-Hydroxy-5-(3-hydroxymethyl-phenyl)-7a-methyl-octahydro-indene-1-carbaldehyde
• CAS NO: 178379-35-6
• Molecular Weight: 288.387
• Mol File: 178379-35-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,3aS,5S,7aR)-3a-Hydroxy-5-(3-hydroxymethyl-phenyl)-7a-methyl-octahydro-indene-1-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3aS,5S,7aR)-3a-Hydroxy-5-(3-hydroxymethyl-phenyl)-7a-methyl-octahydro-indene-1-carbaldehyde(178379-35-6)
• EPA Substance Registry System: (1S,3aS,5S,7aR)-3a-Hydroxy-5-(3-hydroxymethyl-phenyl)-7a-methyl-octahydro-indene-1-carbaldehyde(178379-35-6)

Safety Data

• Hazardous Substances Data: 178379-35-6(Hazardous Substances Data)

Upstream product

• 178379-39-0 (1S,3aS,7aR)-1-hydroxymethyl-3a-hydroxy-7a-methyl-5-perhydroindenone 
• 178379-40-3 (1S,3aS,5S,7aR)-1-hydroxymethyl-5-(3-tert-butyldimethylsilyloxymethylphenyl)-7a-methylperhydroinden-3a,5-diol 
• 178379-44-7 (1S,3aS,5S,7aR)-1-hydroxymethyl-5-(3-tert-butyldimethylsilyloxymethylphenyl)-7a-methylperhydroinden-3a-ol 
• 392234-88-7 (1R,3aS,7aR)-1-hydroxymethyl-5-spiro-2'-(1',3'-dioxolane)-7a-methylperhydroinden-3a-ol 
• 178379-37-8 (3aS,7aR)-1-methylen-3a-hydroxy-7a-methylperhydroindene-5-spiro-2'-(1',3'-dioxolane) 
• 178379-36-7 (3aS,7aS)-3a-hydroxy-5-spiro-2'-(1',3'-dioxolane)-7a-methyl-1-perhydroindenone 
• 392235-07-3 (1S,3aS,5S,7aR)-5-(3-tert-butyldimethylsilyloxymethylphenyl)-3a-hydroxy-7a-methylperhydroindene-1-carboxaldehyde 
• 162240-26-8 C₁₃H₂₀O₄ 
• 103978-12-7 [(3-bromobenzyl)oxy](tert-butyl)dimethylsilane 
• 33879-04-8 (+)-(3aS,7aS)-2,3,3a,4,7,7a-hexahydro-3a-hydroxy-7a-methyl-1H-indene-1,5(6H)-dione 

Relevant articles and documents

Synthesis and inotropic activity of 1-(O-aminoalkyloximes) of perhydroindene derivatives as simplified digitalis-like compounds acting on the Na+,K+-ATpase

A series of 5-substituted (3aS,7aR)-7a-methylperhydroinden-3a-o1 derivatives bearing a 1(S)-(ω-aminoalkoxy)iminoalkyl or -alkenyl substituent was synthesized, starting from the Hajos-Parrish ketol 47, as simplified analogues of very potent 17β-aminoalkylo