261350-46-3 Usage
Uses
Used in Pharmaceutical Industry:
4-Methylisoxazole-5-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential anti-inflammatory, anti-cancer, and antimicrobial properties. Its unique structure allows for the development of new drugs that can target a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Methylisoxazole-5-carboxylic acid is utilized as a building block for the creation of compounds with pesticidal properties, contributing to the development of effective and novel agrochemicals for crop protection.
Used in Medicinal Chemistry Research:
4-Methylisoxazole-5-carboxylic acid is employed as a research tool in medicinal chemistry for exploring its potential role in the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's. Its structural attributes make it a promising candidate for the design of therapeutic agents that could mitigate the effects of these conditions.
Used in Drug Discovery:
As a component in drug discovery processes, 4-Methylisoxazole-5-carboxylic acid aids in the identification and development of new chemical entities with potential therapeutic benefits. Its versatility in chemical synthesis makes it an invaluable asset in the quest for innovative pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 261350-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,3,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 261350-46:
(8*2)+(7*6)+(6*1)+(5*3)+(4*5)+(3*0)+(2*4)+(1*6)=113
113 % 10 = 3
So 261350-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H5NO3/c1-3-2-6-9-4(3)5(7)8/h2H,1H3,(H,7,8)
261350-46-3Relevant academic research and scientific papers
Martins, Marcos A. P.,Flores, Alex F. C.,Bastos, Giovani P.,Sinhorin, Adilson,Bonacorso, Helio G.,Zanatta, Nilo
, p. 293 - 297 (2000)
The one-pot synthesis of ten 5-carboxyisoxazoles from the cyclocondensation of β-alkoxyvinyl trichloromethyl ketones [CCl3C(O)C(R2)=C(R1)OR, where R1, R2=H, Me and R=Me, Et] and 2- trichloroacetyl cyclohexanone with hydroxylamine is reported. This work shows that the trichloromethyl group attached to β-alkoxyvinyl trichloromethyl ketones (a heterocyclic CCC building block) is an excellent carboxyl group precursor.
