69734-92-5

Usage

Type of compound

Complex organic compound

Carboxylic acid group

Present

Acetyloxy group

Present

Methyl ester group

Present

Other functional groups

Several, including a condensed ring system and a hexahydro-14-(hydroxymethyl)-13-methylmoiety

Categorization

Methyl ester

Stereochemistry

[1S-(1a,3b,4E,8ab,13aS,14S)](9CI)

Molecular structure

Contains a condensed ring system and a hexahydro-14-(hydroxymethyl)-13-methylmoiety

Chirality

The compound has chiral centers, as indicated by the stereochemistry notation

Functional groups

Carboxylic acid, acetyloxy, methyl ester, and others within the condensed ring system

Hydrogen bonding

Potential for hydrogen bonding due to the presence of hydroxyl and carbonyl groups

Solubility

Likely to be soluble in organic solvents, such as ethanol or methanol, due to its nonpolar nature

Stability

May be sensitive to heat, light, and moisture due to the presence of multiple functional groups

Reactivity

Potential for reactions involving the carboxylic acid, acetyloxy, and methyl ester groups, as well as other functional groups within the condensed ring system

Biological activity

Unknown, but may have potential applications in pharmaceuticals or other fields due to its complex structure

Synthesis

The synthesis of 13H-3,8a-Methano-1H-azepino[1',2':1,2]pyrrolo[2,3-b]indole-14-carboxylicacid,1-(acetyloxy)-4-ethylidene-2,3,4,5,7,8-hexahydro-14-(hydroxymethyl)-13-methyl-,methyl ester, [1S-(1a,3b,4E,8ab,13aS*,14S*)]- (9CI) would likely involve multiple steps, including the formation of the condensed ring system and the introduction of the various functional groups

Purification

Chromatographic techniques, such as column chromatography or HPLC, may be used to purify the compound from reaction mixtures or to separate diastereomers based on the stereochemistry.