331942-47-3 Usage
Description
2-(2-Furyl)benzoic acid, a derivative of benzoic acid, is a chemical compound characterized by the molecular formula C13H10O4. It features a furan ring and is known for its white to off-white crystalline powder form with a slightly sweet, floral scent. This sparingly soluble in water compound is extensively utilized in the synthesis of pharmaceuticals and as a building block in organic chemistry. Additionally, it has garnered interest for its potential anti-inflammatory and antioxidant properties.
Uses
Used in Pharmaceutical Synthesis:
2-(2-Furyl)benzoic acid is used as a key intermediate in the pharmaceutical industry for the development of various drugs. Its unique chemical structure allows it to be a versatile building block in the creation of new medicinal compounds.
Used in Organic Chemistry Research:
In the field of organic chemistry, 2-(2-Furyl)benzoic acid serves as a valuable research compound. It is employed in the study and development of novel chemical reactions and synthesis pathways, contributing to the advancement of organic chemistry knowledge.
Used in Anti-Inflammatory Applications:
2-(2-Furyl)benzoic acid is studied for its potential as an anti-inflammatory agent. Its properties are being investigated for their ability to reduce inflammation, which could be beneficial in the treatment of various inflammatory conditions.
Used in Antioxidant Applications:
The antioxidant potential of 2-(2-Furyl)benzoic acid is also under investigation. Its capacity to neutralize free radicals may offer protective effects against oxidative stress, which is implicated in numerous diseases and aging processes.
Used in Chemical Synthesis:
2-(2-Furyl)benzoic acid is utilized in the synthesis of various chemical compounds, including other benzoic acid derivatives and furan-containing molecules. Its reactivity and structural features make it a useful component in the creation of specialty chemicals for different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 331942-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,9,4 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 331942-47:
(8*3)+(7*3)+(6*1)+(5*9)+(4*4)+(3*2)+(2*4)+(1*7)=133
133 % 10 = 3
So 331942-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O3/c12-11(13)9-5-2-1-4-8(9)10-6-3-7-14-10/h1-7H,(H,12,13)
331942-47-3Relevant articles and documents
Palladium-catalyzed intramolecular aromatic C-H acylation of 2-arylbenzoyl fluorides
Hayakawa, Kazuki,Ikai, Kana,Ogiwara, Yohei,Sakai, Norio,Sakurai, Yuka
, p. 1882 - 1893 (2021/08/13)
The catalytic intramolecular cyclization of acyl fluorides using a Pd(OAc)2/PCy3 system is described. A wide range of 2-arylbenzoyl fluoride derivatives can be used as fluorenone precursors and the reaction proceeds via an intramolecular coupling between aromatic C-H bonds with acyl C-F bonds. The reaction can be applied to the synthesis of indenofluorenedione derivatives and to the construction of other molecules with fivemembered rings.
Synthesis and biological evaluation of benzimidazole derivatives as potent AMP-activated protein kinase activators
Charton, Julie,Girault-Mizzi, Sophie,Debreu-Fontaine, Marie-Ange,Foufelle, Fabienne,Hainault, Isabelle,Bizot-Espiard, Jean-Guy,Caignard, Daniel-Henri,Sergheraert, Christian
, p. 4490 - 4518 (2007/10/03)
Design, synthesis and structure-activity relationships of benzimidazole derivatives as activators of the AMP-activated protein kinase (AMPK) are presented in this paper. AMPK is the central component of a protein kinase cascade that plays a key role in the regulation of energy balance. Once activated, AMPK initiates a series of responses that are aimed at restoring the energy balance of the cell and recent studies have indicated that AMPK plays an important role in regulation of the whole-body energy metabolism. The following study based on the lead compound S27847 involved modification of three regions of this compound. Preliminary structure-activity relationships are being described.
