60715-04-0

Basic information

• Product Name: 1-[5-hydroxy-7-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-chromen-6-yl]ethanone
• Synonyms: 1-[5-hydroxy-7-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-chromen-6-yl]ethanone
• CAS NO: 60715-04-0
• Molecular Weight: 316.397
• Mol File: 60715-04-0.mol

Chemical Properties

• CAS DataBase Reference: 1-[5-hydroxy-7-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-chromen-6-yl]ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[5-hydroxy-7-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-chromen-6-yl]ethanone(60715-04-0)
• EPA Substance Registry System: 1-[5-hydroxy-7-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-chromen-6-yl]ethanone(60715-04-0)

Safety Data

• Hazardous Substances Data: 60715-04-0(Hazardous Substances Data)

Upstream product

• 65490-09-7 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone 
• 480-66-0 2,4,6-trihydroxyacetophenone 
• 404597-94-0 1-(2-methoxy-4,6-bis(methoxymethoxy)phenyl)ethan-1-one 
• 3602-54-8 4,6-dihydroxy-2-methoxyacetophenone 
• 5392-40-5 (E/Z)-3,7-dimethyl-2,6-octadienal 

Downstream Products

• 93208-46-9 boesenbergin B 

Relevant articles and documents

EDDA-catalyzed rapid synthetic routes for biologically interesting polycycles bearing citrans and chalcones: the first total synthesis of sumadain A

An efficient and concise synthetic route for biologically interesting polycycles bearing citran and chalcone nuclei was developed starting from a variety of trihydroxybenzenes with substituents on the ring. The key strategies involved an ethylenediamine diacetate-catalyzed cyclization by a domino aldol-type/electrocyclization/H-shift/hetero Diels-Alder reaction of trihydroxybenzenes and citral or trans,trans-farnesal. This methodology was applied successfully to the synthesis of three natural products, desbenzylidenerubramin, rubraine, sumadain A, and their unnatural derivatives.

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Loss of neuronal tissue is a hallmark of age-related neurodegenerative diseases. Since adult neurogenesis has been confirmed in the human brain, great interest has arisen in substances stimulating the endogenous neuronal regeneration mechanism based on ad

Chromane-like cyclic prenylflavonoids for the medical intervention in neurological disorders

The present invention relates to certain chromane-like cyclic prenylflavonoids, in particular the compounds of formulae (I), (II) and (III) as described and defined herein, for use in the treatment or prevention of a neurological disorder, as well as their use in promoting neuronal differentiation, neurite outgrowth and neuroprotection.

Concise total synthesis of biologically interesting pyranochalcone natural products: Citrunobin, boesenbergin A, boesenbergin B, xanthohumol C, and glabrachromene

New and efficient synthetic approaches to the biologically interesting natural products citrunobin, boesenbergins A and B, xanthohumol C, and glabrachromene are described. The key strategies involve ethylenediamine diacetate catalyzed benzopyran formation