134541-06-3 Usage
Uses
Used in Pharmaceutical Industry:
5-TERT-BUTYL-ISOXAZOLE-4-CARBOXYLIC ACID is used as a building block for the synthesis of various pharmaceutical drugs due to its unique chemical properties and reactivity.
Used in Organic Synthesis:
5-TERT-BUTYL-ISOXAZOLE-4-CARBOXYLIC ACID is used as an intermediate in the synthesis of other organic compounds, leveraging its carboxylic acid derivative nature to facilitate the formation of desired products.
Used in Anti-Inflammatory Applications:
5-TERT-BUTYL-ISOXAZOLE-4-CARBOXYLIC ACID is used as an anti-inflammatory agent, capitalizing on its inherent properties to reduce inflammation and alleviate associated symptoms.
Used in Antimicrobial Applications:
5-TERT-BUTYL-ISOXAZOLE-4-CARBOXYLIC ACID is used as an antimicrobial agent, harnessing its ability to inhibit the growth of microorganisms, thus serving as a potential component in treatments for various infections.
Check Digit Verification of cas no
The CAS Registry Mumber 134541-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,4 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134541-06:
(8*1)+(7*3)+(6*4)+(5*5)+(4*4)+(3*1)+(2*0)+(1*6)=103
103 % 10 = 3
So 134541-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO3/c1-8(2,3)6-5(7(10)11)4-9-12-6/h4H,1-3H3,(H,10,11)
134541-06-3Relevant academic research and scientific papers
Reaction of 2-Dimethylaminomethylene-1,3-diones with Dinucleophiles. X. Synthesis of 5-Substituted Ethyl or Methyl 4-Isoxazolecarboxylates and Methyl 4-(2,2-Dimethyl-1-oxopropyl)-5-isoxazolecarboxylate
Schenone, Pietro,Fossa, Paola,Menozzi, Giulia
, p. 453 - 457 (2007/10/02)
Reaction of ethyl or methyl 2-dimethylaminomethylene-3-oxoalkanoates with hydroxylamine hydrochloride in methanol solution afforded in high yields the relative esters of 5-substituted 4-isoxazolecarboxylic acids II.These esters were hydrolyzed generally with concentrated hydrochloric acid-acetic acid mixtures to the corresponding carboxylic acids in satisfactory yields.Ethyl or methyl esters II isomerized with sodium ethoxide or methoxide, respectively, to the corresponding esters or hemiesters of 2-cyano-3-oxoalkanoic acids generally in excellent to satisfactory yields.Reaction of methyl 5,5-dimethyl-3-dimethylaminomethylene-2,4-dioxohexanoate with hydroxylamine hydrochloride afforded in moderate yield methyl 4-(2,2-dimethyl-1-oxopropyl)-5-isoxazolecarboxylate, which was converted by acid hydrolysis as above to 4-t-butyl-4-hydroxyfuroisoxazol-6-(4H)-one.
