108124-17-0 Usage
Description
2-METHYL-5-PHENYLFURAN-3-CARBOXYLIC ACID is a furan derivative with the molecular formula C13H10O3, featuring a carboxylic acid functional group. It is a white to off-white crystalline solid with a melting point of approximately 148-150°C. This chemical compound has potential applications in pharmaceuticals, organic synthesis, and the development of new drugs.
Uses
Used in Pharmaceutical Industry:
2-METHYL-5-PHENYLFURAN-3-CARBOXYLIC ACID is used as an intermediate in the synthesis of various pharmaceutical compounds due to its unique chemical structure and reactivity.
Used in Organic Synthesis:
2-METHYL-5-PHENYLFURAN-3-CARBOXYLIC ACID is used as a building block in the preparation of complex organic molecules, contributing to the development of novel chemical entities with potential applications in various fields.
Used in Drug Development:
2-METHYL-5-PHENYLFURAN-3-CARBOXYLIC ACID is used as a potential candidate for the development of new drugs, leveraging its chemical properties to target specific biological pathways or mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 108124-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,2 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108124-17:
(8*1)+(7*0)+(6*8)+(5*1)+(4*2)+(3*4)+(2*1)+(1*7)=90
90 % 10 = 0
So 108124-17-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O3/c1-8-10(12(13)14)7-11(15-8)9-5-3-2-4-6-9/h2-7H,1H3,(H,13,14)/p-1
108124-17-0Relevant articles and documents
Discovery and hit-to-lead optimization of novel allosteric glucokinase activators
Lang, Martin,Seifert, Markus H.-J.,Wolf, Kristina K.,Aschenbrenner, Andrea,Baumgartner, Roland,Wieber, Tanja,Trentinaglia, Viola,Blisse, Marcus,Tajima, Nobumitsu,Yamashita, Tokuyuki,Vitt, Daniel,Noda, Hitoshi
, p. 5417 - 5422 (2011/10/12)
We report on a hit generation and hit-to-lead program of a novel class of glucokinase activators (GKAs). Hit compounds, activators at low glucose concentration only were identified by vHTS. Scaffold modification reliably afforded activators also at high s
