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(5-oxo-2,2-diphenyltetrahydrofuran-3-yl)acetic acid is a chemical compound with the molecular formula C20H18O4, belonging to the class of heterocyclic organic compounds. It features a tetrahydrofuran ring fused with two phenyl groups and a carbonyl group at the 5th position, along with an acetic acid functional group. This unique structure endows the compound with potential applications in organic synthesis and medicinal chemistry.

7496-07-3

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7496-07-3 Usage

Uses

Used in Pharmaceutical Research:
(5-oxo-2,2-diphenyltetrahydrofuran-3-yl)acetic acid is used as a compound of interest in pharmaceutical research due to its demonstrated anti-inflammatory and analgesic properties. Its unique structure may contribute to the development of novel therapeutic agents for various conditions.
Used in Organic Synthesis:
In the field of organic synthesis, (5-oxo-2,2-diphenyltetrahydrofuran-3-yl)acetic acid serves as a valuable intermediate or building block for the creation of more complex molecules. Its distinct functional groups and ring systems can be utilized in various synthetic pathways to produce a wide range of compounds with diverse applications.
Further research is necessary to fully explore and understand the potential uses and effects of (5-oxo-2,2-diphenyltetrahydrofuran-3-yl)acetic acid in these and other applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7496-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7496-07:
(6*7)+(5*4)+(4*9)+(3*6)+(2*0)+(1*7)=123
123 % 10 = 3
So 7496-07-3 is a valid CAS Registry Number.

7496-07-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-oxo-2,2-diphenyloxolan-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7496-07-3 SDS

7496-07-3Downstream Products

7496-07-3Relevant academic research and scientific papers

Synthesis of terpenylic acid and its analogues by oxidative cleavage and lactonization of cyclopentenyl carbinols

Dao, Pham Duy Quang,Park, Jun-Hyun,Lim, Ho-Jin,Cho, Chan Sik

, p. 1885 - 1889 (2021/11/17)

Cyclopentenyl carbinols are oxidatively cleaved and cyclized into a class of terpenylic acid analogues in the presence of oxone and sodium periodate in good yields. Graphical abstract: [Figure not available: see fulltext.]

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