88391-19-9

Usage

Naphthalene ring structure

The presence of a naphthalene ring indicates that the compound has a fused benzene ring system, which may contribute to its stability and potential biological activity.

Carboxylic acid group

The carboxylic acid group is a functional group consisting of a carbonyl group (C=O) and a hydroxyl group (-OH) bonded to the same carbon atom. This group is important for the compound's acidity and may be involved in hydrogen bonding interactions.

Multiple hydroxyl groups

The presence of multiple hydroxyl (-OH) groups suggests that the compound may be soluble in water and may be involved in hydrogen bonding interactions.

Ketone functional groups

The presence of ketone groups (C=O) suggests that the compound may have some degree of lipophilicity, which may affect its pharmacokinetics and biological activity.

Ethyl group

The presence of an ethyl group (-CH2-CH3) indicates that the compound has a degree of lipophilicity, which may affect its pharmacokinetics and biological activity.

Methyl ester

The presence of a methyl ester group (-COOCH3) suggests that the compound has a degree of lipophilicity, which may affect its pharmacokinetics and biological activity.

cis-Configuration

The cis-configuration indicates that the hydroxyl and ketone groups are on the same side of the naphthalene ring, which may affect the compound's biological activity and pharmacokinetics.

Pharmaceutical properties

The compound has potential pharmaceutical properties, which means it may be used in the development of pharmaceutical drugs or could potentially have biological effects itself.

Further research needed

Further research is needed to fully understand the properties and potential applications of this complex compound.

Upstream product

• 74188-46-8 4,5-Dihydroxy-9,10-dioxo-3-(3-oxopentyl)anthracene-2-acetic Acid, Methyl Ester 
• 88365-16-6 3-(2-Diazo-acetyl)-1-hydroxy-8-methoxy-2-(3-oxo-pentyl)-anthraquinone 
• 88365-11-1 3-(Acetoxymethyl)-1-(2,2-dimethylpropionyloxy)-8-methoxy-2-(3-oxopentyl)-9,10-anthrachinon 
• 76964-28-8 1-formyl-butan-2-one ethylene acetal 
• 81418-41-9 1-(1-hydroxy-4,8-dimethoxynaphthalen-2-yl)ethanone 
• 95456-09-0 3-acetyl-1,5-dimethoxy-4-methoxymethoxynaphthalene 
• 135106-36-4 4-Hydroxy-5,8-dihydro-5,8-dioxo-3-(3-oxopentyl)-naphthaleneactic Acid, Methyl Ester 
• 97453-40-2 [9-(tert-Butyl-dimethyl-silanyloxy)-10-hydroxy-5-methoxy-4-oxo-3-(3-oxo-pentyl)-1,2,3,4-tetrahydro-anthracen-2-yl]-acetic acid methyl ester 
• 89101-88-2 methyl (6a-SR,9-RS,10-RS,10a-RS)-9-ethyl-12-t-butyldimethylsilyloxy-5,9-dihydroxy-4-methoxy-6-oxo-6,6a,7,8,9,10,10a,11-octahydronaphthacene-10-carboxylate 
• 89101-85-9 methyl 4-(1'-t-butyldimethylsilyloxy-4'-hydroxy-5'-methoxy-3'-(5''-oxoheptanoyl)-naphth-2'-yl)-2-butenoate 
• 95455-97-3 methyl 4-(4'-hydroxy-5'-methoxy-1'-oxo-3'-(5''-oxoheptanoyl)-1',2'-dihydronaphth-2'-yl)-2-butenoate 
• 95455-82-6 methyl (6a-SR,9-RS,10-RS,10a-RS)-9-ethyl-5,9,12-trihydroxy-4-methoxy-6-oxo-6,6a,7,8,9,10,10a,11-octahydronaphthacene 
• 89101-83-7 3-(5,5-ethylenedioxy-2-heptenoyl)-1,5-dimethoxy-4-methoxymethoxynaphthalene 
• 95456-15-8 3-(5,5-ethylenedioxyheptanoyl)-1,5-dimethoxy-4-methoxymethoxynaphthalene 

Downstream Products

• 16234-96-1 t-2-Ethyl-1,2,3,4,6,11-hexahydro-c-2,t-4,5,7-tetrahydroxy-6,11-dioxo-r-1-naphthacencarbonsaeure-methylester 
• 16234-96-1 (+/-)-Aklavinon-I 

Relevant academic research and scientific papers

SYNTHESES OF (+/-)-AKLAVINONES. APPLICATION OF THE STEREOCONTROLLED "ZIPPER" BICYCLO-CYCLIZATION REACTION

Efficient syntheses of (+/-)-aklavinones; (+/-)-aklavinone (1), (+/-)-auramycinone (2), and (+/-)-13-methylaklavinone (3), are described.A key process of the tetracyclic ring construction in these syntheses is a stereocontrolled "zipper" bicyclo-cyclizati

An Efficient Total Synthesis of (+/-)-Aklavinone

An 11-step total synthesis of (+/-)-aklavinone from 1,3-cyclohexadione is reported.The key steps include a Diels-Alder condensation of 3 and 4 and the stereoselective aldol condensation of 21 to 22.The overall yield is ca. 13percent.