55923-05-2

Basic information

• Product Name: 1-(1-(DIFLUOROBORYL)OXY-3,4-DIHYDRO-NAPHTHALEN-2-YL)-ETHANONE INNER COMPLEX
• Synonyms: 1-(1-(DIFLUOROBORYL)OXY-3,4-DIHYDRO-NAPHTHALEN-2-YL)-ETHANONE INNER COMPLEX;1-(1-(Difluoroboryl)oxy-3,4-dihydro-naphthalen-2-yl)-ethanone;Innercomplex
• CAS NO: 55923-05-2
• Molecular Formula: C₁₂H₁₁BF₂O₂
• Molecular Weight: 236.02
• Mol File: 55923-05-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(1-(DIFLUOROBORYL)OXY-3,4-DIHYDRO-NAPHTHALEN-2-YL)-ETHANONE INNER COMPLEX(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-(DIFLUOROBORYL)OXY-3,4-DIHYDRO-NAPHTHALEN-2-YL)-ETHANONE INNER COMPLEX(55923-05-2)
• EPA Substance Registry System: 1-(1-(DIFLUOROBORYL)OXY-3,4-DIHYDRO-NAPHTHALEN-2-YL)-ETHANONE INNER COMPLEX(55923-05-2)

Safety Data

• Hazardous Substances Data: 55923-05-2(Hazardous Substances Data)

Usage

Description

1-(1-(Difluoroboryl)oxy-3,4-dihydro-naphthalen-2-yl)-ethanone inner complex is a chemical compound characterized by its complex structure, featuring a naphthalene ring and a difluoroboryl group. 1-(1-(DIFLUOROBORYL)OXY-3,4-DIHYDRO-NAPHTHALEN-2-YL)-ETHANONE INNER COMPLEX is known for its unique reactivity and properties, which distinguish it from other similar compounds. The inner complex structure and the presence of the difluoroboryl group make it a valuable tool for chemical research and development, as well as a promising candidate for various chemical and industrial processes.

Uses

Used in Chemical Research and Development:
1-(1-(Difluoroboryl)oxy-3,4-dihydro-naphthalen-2-yl)-ethanone inner complex is used as a building block for the synthesis of other compounds. Its unique structure and reactivity make it a valuable asset in the development of new chemical compounds and materials.
Used in Catalytic Reactions:
The presence of the difluoroboryl group in the compound allows for opportunities in catalytic reactions. 1-(1-(Difluoroboryl)oxy-3,4-dihydro-naphthalen-2-yl)-ethanone inner complex can be used as a catalyst or a catalyst precursor in various chemical transformations, potentially leading to the development of more efficient and environmentally friendly processes.
Used in Industrial Applications:
As a promising candidate for a wide range of chemical and industrial processes, 1-(1-(Difluoroboryl)oxy-3,4-dihydro-naphthalen-2-yl)-ethanone inner complex can be utilized in various industries, such as pharmaceuticals, materials science, and chemical manufacturing, to develop new products and improve existing processes.

Upstream product

• 17216-08-9 2-acetyl-1-tetralone 
• 108-24-7 acetic anhydride 
• 109-63-7 trifluoroborane diethyl ether 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 1233879-00-9 C₁₃H₁₃BF₂O₃ 
• 917-54-4 methyllithium 
• 1822-00-0 trimethylsilylmethyllithium 

Relevant articles and documents

Selective addition of organolithium reagents to BF2-chelates of β-ketoesters

A short, mild, and highly chemoselective addition of organolithium reagents to a BF2 complex of 3-oxopropanoates has been developed. The methodology allows straightforward preparation of various 1,3-dioxa-BF 2 complexes and subsequently leads to the formation of 1,3-diketones starting from the corresponding 3-oxopropanoates.

Polycyclic dioxaborin complexes

A process for the production of partially saturated gamma-pyrones of the general formula I: SPC1 wherein R represents hydrogen, hydroxy, lower alkyl, or lower alkoxy and n represents 1 or 2, by reacting a suitably substituted tetralone (IIa) or indanone (IIb) with a boron trifluoride compound and acetic anhydride to obtain intermediate boron complexes III, which are reacted with a Vilsmeier reagent prepared from phosphorus oxychloride and dimethylformamide to obtain the partially saturated gamma-pyrones of formula I. The gamma-pyrones I have anti-allergy and anti-secretory activity.