36508-91-5

Basic information

• Product Name: (R)-3-(3-oxo-1-phenylbutyl)-4-sodiooxy-2H-1-benzopyran-2-one
• Synonyms: (R)-3-(3-oxo-1-phenylbutyl)-4-sodiooxy-2H-1-benzopyran-2-one;4-(Sodiooxy)-3-[(R)-3-oxo-1-phenylbutyl]-2H-1-benzopyran-2-one
• CAS NO: 36508-91-5
• Molecular Formula: C19H15NaO4
• Molecular Weight: 330.30977
• EINECS: 253-078-5
• Mol File: 36508-91-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-3-(3-oxo-1-phenylbutyl)-4-sodiooxy-2H-1-benzopyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-(3-oxo-1-phenylbutyl)-4-sodiooxy-2H-1-benzopyran-2-one(36508-91-5)
• EPA Substance Registry System: (R)-3-(3-oxo-1-phenylbutyl)-4-sodiooxy-2H-1-benzopyran-2-one(36508-91-5)

Safety Data

• Hazardous Substances Data: 36508-91-5(Hazardous Substances Data)

Usage

General Description

"(R)-3-(3-oxo-1-phenylbutyl)-4-sodiooxy-2H-1-benzopyran-2-one" is a chemical compound with a complex structure. It contains a benzopyran ring and a phenylbutyl moiety. The compound also has a keto group and a sodium oxy moiety. It is a derivative of 2H-1-benzopyran-2-one and is optically active due to the presence of the (R) configuration. (R)-3-(3-oxo-1-phenylbutyl)-4-sodiooxy-2H-1-benzopyran-2-one may have potential pharmaceutical properties and could be used in the synthesis of various organic compounds. Its precise uses and applications would depend on further research and testing.

Upstream product

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Relevant articles and documents

A facile synthesis of non-aqueous LiPO2F2 solution as the electrolyte additive for high performance lithium ion batteries

Constructing a reliable and favorable electrode-electrolyte interface is crucial to utilize the exceptional energy storage capability in commercial lithium-ion batteries. Here, we report a facile synthesis approach for the lithium difluorophosphate (LiPO2F2) solution as an effective film-forming additive via direct adding the Li2CO3 into LiPF6 solution at 45 °C. Benefiting from the significantly reduced interface resistance (RSEI) and charge transfer impedance (Rct) of both the cathode and anode by adding the prepared LiPO2F2 solution into a baseline electrolyte, the cycling performance of the graphite||LiNi0.5Mn0.3Co0.2O2 pouch cell is remarkably improved under all-climate condition.

Champ de forces de symetrie locale des composes oxyfluores du phosphore(V)-I. Les difluorodioxophosphates (DFP) alcalins

Alkali phosphorofluoridates (DFP) were prepared by reaction between phosphoryl difluoride oxide P2O3F4 and alkali fluorides.The caesium salt was obtained by reaction between HPO2F2 and caesium chloride.The aim was to establish a coherent description of the various vibrational modes of the PO2F2- ion, so as to use it for more complex molecules involving either of the PO2 and PF2 groups.For that purpose a local symmetric force field (LSFF) was chosen and good agreement found between calculated and observed frequencies.This investigation provided force constant values for the PO2F2- ion in RbPO2F2, and enabled us to test the transferability of the force field to the DFP whose cristallographic structures are known.