3565-77-3

Usage

Uses

Used in Organic Synthesis:
2,5-dimethoxy-3-tridecyl-cyclohexa-2,5-diene-1,4-dione is used as a building block or intermediate in the synthesis of more complex organic molecules. Its unique structure and reactivity make it a valuable component in the development of novel organic compounds with specific properties and functions.
Used in Pharmaceutical Industry:
2,5-dimethoxy-3-tridecyl-cyclohexa-2,5-diene-1,4-dione is used as a potential active pharmaceutical ingredient (API) or as a key intermediate in the synthesis of new drugs. Its unique molecular structure may offer novel therapeutic properties, such as targeting specific biological pathways or exhibiting selective interactions with biological targets.
Used in Materials Science:
2,5-dimethoxy-3-tridecyl-cyclohexa-2,5-diene-1,4-dione is used as a component in the development of new materials with specific properties, such as improved stability, enhanced reactivity, or unique physical characteristics. Its incorporation into materials may lead to the creation of innovative products with applications in various industries, including electronics, coatings, and adhesives.

InChI:InChI=1/C21H34O4/c1-4-5-6-7-8-9-10-11-12-13-14-15-17-20(23)19(24-2)16-18(22)21(17)25-3/h16H,4-15H2,1-3H3

Upstream product

• 765-09-3 1-bromotridecane 
• 219144-65-7 1,2,4,5-tetramethoxy-3-tridecylbenzene 
• 2441-46-5 1,2,4,5-tetramethoxybenzene 
• 30225-87-7 2,4,5-trimethoxyphenyl formate 
• 4460-86-0 asaraldehyde 

Downstream Products

• 21772-36-1 3-Tridecyl-2,5-bis-(isopropylamino)-p-benzochinon 
• 21772-30-5 2,5-bis-methylamino-3-tridecyl-[1,4]benzoquinone 
• 19833-82-0 2-hydroxy-5-methoxy-3-tridecylcyclohexa-2,5-diene-1,4-dione 
• 573-40-0 rapanone 
• 1600526-60-0 tert-butyl 4-((4-methoxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienyl)(methyl)amino)-butanoate 
• 1600526-59-7 tert-butyl 4-((4-hydroxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienyl)(methyl)amino)-butanoate 
• 21772-33-8 5-(dimethylamino)-2-methoxy-3-tridecylcyclohexa-2,5-diene-1,4-dione 
• 1600526-58-6 5-(dimethylamino)-2-hydroxy-3-tridecylcyclohexa-2,5-diene-1,4-dione 
• 1600526-57-5 hexyl 4-((4-methoxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienyl)(methyl)amino)butanoate 
• 1600526-56-4 hexyl 4-((4-hydroxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienyl)(methyl)amino)butanoate 
• 1600526-55-3 hexyl 4-(4-methoxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienylamino)butanoate 
• 1600526-54-2 hexyl 4-(4-hydroxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienylamino)butanoate 
• 1600526-53-1 butyl 4-(4-methoxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienylamino)butanoate 
• 1600526-52-0 butyl 4-(4-hydroxy-3,6-dioxo-5-tridecylcyclohexa-1,4-dienylamino)butanoate 

Relevant academic research and scientific papers

Design, synthesis and α-glucosidase inhibition study of novel embelin derivatives

Embelin is a naturally occurring para-benzoquinone isolated from Embelia ribes (Burm. f.) of the Myrsinaceae family. It was first discovered to have potent inhibitory activity (IC50 = 4.2 μM) against α-glucosidase in this study. Then, four seri

Novel series of benzoquinones with high potency against 5-lipoxygenase in human polymorphonuclear leukocytes

5-Lipoxygenase (5-LO) is a potential target for pharmacological intervention with various inflammatory and allergic diseases. Starting from the natural dual 5-LO/microsomal prostaglandin E2 synthase (mPGES)-1 inhibitor embelin (2,5-dihydroxy-3-

MULTIFUNCTIONAL RADICAL QUENCHERS

The invention provides a compound of formula (I): [insert formula (I)] wherein X, Y, and R1-R4 have any of the values defined in the specification, and salts thereof, as well as compositions comprising the compounds or salts. The compounds are useful for treating diseases associated with impaired mitochondrial function in an animal.

Synthesis and biological activities of N-(3-Carboxylpropyl)-5-amino-2- hydroxy-3-tridecyl-1,4-benzoquinone and analogues

The synthesis of benzoquinone natural product 2 and three analogues is described. The synthesized compounds were tested for their ability to protect Friedreich's ataxia (FRDA) lymphocytes from induced oxidative stress. One of the analogues (3) conferred c

First synthesis of N-(3-carboxylpropyl)-5-amino-2-hydroxy-3-tridecyl-1,4- benzoquinone, an unusual quinone isolated from Embelia ribes

(Chemical Equation Presented) The first synthesis of the unusual nitrogen-containing 3-alkyl-1,4-benzoquinone, N-(3-carboxylpropyl)-5-amino-2- hydroxy-3-tridecyl-1,4-benzoquinone, isolated from Embelia ribes, is reported. The key steps are a microwave-ass

Total synthesis of maesanin and analogues

An efficient total synthesis of maesanin and related quinones is reported, through direct alkylation of 1,2,4,5-tetramethoxybenzene with alkylbromides, followed by oxidation with ceric ammonium nitrate (CAN) which provokes formation of the quinone and dep