24909-95-3

24909-95-3 - Names and Identifiers

Name	(1'R,3R,7'aβ)-1'β,7'α-Dihydroxy-3'aβ,4'β-dimethyl-4-methylenespiro[oxolane-3,2'-hydrindane]-2-one
Synonyms	Fukinolidol Fukinolidiol Bakkenolide III (2R,3aα)-2'-Oxo-4'-methylene-7α,7aα-dimethylspiro[hydrindane-2,3'-oxolane]-3α,4β-diol (1'R,3R,7'aβ)-1'β,7'α-Dihydroxy-3'aβ,4'β-dimethyl-4-methylenespiro[oxolane-3,2'-hydrindane]-2-one Spiro[furan-3(2H),2'-[2H]inden]-2-one, decahydro-1',7'-dihydroxy-3'a,4'-dimethyl-4-methylene-, (1'R,2'R,3'aR,4'S,7'S,7'aR)- (1'R,3R)-1',3',3'a,4,4',5,5',6',7',7'aβ-Decahydro-1'β,7'α-dihydroxy-3'aβ,4'β-dimethyl-4-methylenespiro[furan-3(2H),2'-[2H]inden]-2-one
CAS	24909-95-3

24909-95-3 - Physico-chemical Properties

Molecular Formula	C15H22O4
Molar Mass	266.33
Storage Condition	2-8℃

24909-95-3 - Introduction

The compound (1'R,3R,7'aβ)-1'β,7'α-Dihydroxy-3 'aβ,4'β-dimethyl-4-methylenespiro[oxolane-3,2 '-hydrindane]-2-one (often also known as (1'R,3R,7'aβ)-dihydroxy-3 'aβ,4'β-dimethyl-4-methylenespiro[oxolane-3,2'-hydrindane]-2-one) is an organic compound. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-chemical formula: C14H18O4
-Molecular weight: 250.29g/mol
-Appearance: white or off-white crystalline powder
-Melting point: About 140-143 ° C
-Solubility: Soluble in some organic solvents, such as ethanol and dimethylformamide

Use:
The compound is of certain importance in the field of medicinal chemistry and drug synthesis, and can be used to synthesize a variety of biologically active molecules and drugs. Due to its specific stereo structure and chemical reactivity, it can be used as an intermediate for the synthesis of complex natural products or drug molecules containing fused ring structures. In addition, it can also be used to synthesize compounds containing α,β-saturated ketone structure, which has important application value in biological activity research.

Method:
Because the compound is a relatively complex organic molecule, its synthesis requires a multi-step reaction. A common synthetic method is to carry out step-by-step transformation from suitable starting compounds through chemical reactions, such as oxidation, reduction, cyclization and ketone synthesis to build the skeleton and stereo structure of the target molecule.

Safety Information:
For specific toxicity and safety data, please refer to the relevant chemical literature and safety data. When handling the compound in the laboratory, strict compliance with the relevant chemical safety procedures and appropriate personal protective measures should be taken.

Last Update：2024-04-09 21:04:16