672904-14-2

Basic information

• Product Name: 4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydro-
• Synonyms: 4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydro-;6-Ethyl-2,3-dihydro-4H-chroMen-4-one;6-ethyl-2,3-dihydro-4H-1-Benzopyran-4-one;7-ethyl-1,2,3,4-tetrahydronaphthalen-1-one
• CAS NO: 672904-14-2
• Molecular Formula: C11H12O2
• Molecular Weight: 176.21178
• Mol File: 672904-14-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydro-(672904-14-2)
• EPA Substance Registry System: 4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydro-(672904-14-2)

Safety Data

• Hazardous Substances Data: 672904-14-2(Hazardous Substances Data)

Usage

Uses

As the specific applications and uses of 4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydroare still under investigation, the following potential uses are based on the general properties of Benzopyran compounds and their possible applications in various industries:
Used in Pharmaceutical Industry:
4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydrocould be used as a pharmaceutical compound for [application reason], such as targeting specific biological pathways or exhibiting therapeutic effects. The exact application reason would depend on the results of ongoing research and the compound's demonstrated properties.
Used in Chemical Research:
4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydromay be utilized as a research compound in the field of organic chemistry, where it could be studied for its chemical properties, reactivity, or potential use in the synthesis of other compounds.
Used in Material Science:
In the field of material science, 4H-1-Benzopyran-4-one, 6-ethyl-2,3-dihydrocould be explored for its potential applications in the development of new materials with unique properties, such as improved stability, conductivity, or optical characteristics.

Upstream product

• 358351-16-3 3-(4-ethyl-phenoxy)-propionic acid 
• 24539-92-2 3-ethyl-6-hydroxyacetophenone 
• 259532-90-6 1-(3-bromo-5-ethyl-2-hydroxyphenyl)ethan-1-one 

Relevant articles and documents

Redox-Neutral Coupling between Two C(sp3)?H Bonds Enabled by 1,4-Palladium Shift for the Synthesis of Fused Heterocycles

The intramolecular coupling of two C(sp3)?H bonds to forge a C(sp3)?C(sp3) bond is enabled by 1,4-Pd shift from a trisubstituted aryl bromide. Contrary to most C(sp3)?C(sp3) cross-dehydrogenative couplings, this reaction operates under redox-neutral conditions, with the C?Br bond acting as an internal oxidant. Furthermore, it allows the coupling between two moderately acidic primary or secondary C?H bonds, which are adjacent to an oxygen or nitrogen atom on one side, and benzylic or adjacent to a carbonyl group on the other side. A variety of valuable fused heterocycles were obtained from easily accessible ortho-bromophenol and aniline precursors. The second C?H bond cleavage was successfully replaced with carbonyl insertion to generate other types of C(sp3)-C(sp3) bonds.

METHODS OF TREATMENT OF AMYLOIDOSIS USING BI-CYCLIC ASPARTYL PROTEASE INHIBITORS

The invention relates to novel compounds and methods of treating diseases, disorders, and conditions associated with amyloidosis. Amyloidosis refers to a collection of diseases, disorders, and conditions associated with abnormal deposition of A-beta protein.