28730-32-7 Usage
Uses
Used in Pharmaceutical Industry:
2,4,5-Trimethyl-3-furoic acid is used as an intermediate in the synthesis of pharmaceuticals for its potential anti-inflammatory and antioxidant properties. It aids in the development of treatments for various diseases and conditions, enhancing the therapeutic efficacy of medications.
Used in Agricultural Chemical Industry:
In the agricultural sector, 2,4,5-Trimethyl-3-furoic acid is used as a building block in the production of agricultural chemicals. Its chemical properties contribute to the development of effective and stable agrochemicals, supporting crop protection and enhancement.
Used in Organic Compounds Production:
2,4,5-Trimethyl-3-furoic acid is utilized as a key component in the synthesis of other organic compounds. Its versatility and stability make it a valuable precursor in the creation of a wide range of organic substances for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 28730-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,3 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28730-32:
(7*2)+(6*8)+(5*7)+(4*3)+(3*0)+(2*3)+(1*2)=117
117 % 10 = 7
So 28730-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O3/c1-4-5(2)11-6(3)7(4)8(9)10/h1-3H3,(H,9,10)
28730-32-7Relevant academic research and scientific papers
Design, synthesis and antifungal activity of novel furancarboxamide derivatives
Wen, Fang,Jin, Hong,Tao, Ke,Hou, Taiping
, p. 244 - 251 (2016/05/24)
Twenty-seven novel furancarboxamide derivatives with a diphenyl ether moiety were synthesized and evaluated for their antifungal activity against Rhizoctonia solani, Botrytis cirerea, Valsa Mali and Sphaceloma ampelimum. Antifungal bioassay results indicated that most compounds had good or excellent fungicidal activities for R. solani and S. ampelimum at 20 mg L-1. Among synthesized compounds, compound 18e showed a greater inhibitory effect against S. ampelimum, with half maximal effective concentration (EC50) values of 0.020 mg L-1. This strong activity rivals currently used commercial fungicides, such as Boscalid and Carbendazim, and has great potential as a lead compound for future development of novel fungicides.
Furan-3-carboxamide derivatives and method of preparing same
-
, (2008/06/13)
A broad class of furan-3-Carboxamide derivatives, including many novel compounds, can be made reliably and in good yields by a novel one step reaction between an α-hydroxyketone and an acetamide in the presence of a Friedel-Crafts agent in an inert solvent. The broad class of derivatives has fungicidal and insecticidal utility.
