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<(5-methyl-3-isoxazolyl)amino>oxoacetic acid sodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99356-64-6

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99356-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99356-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,5 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99356-64:
(7*9)+(6*9)+(5*3)+(4*5)+(3*6)+(2*6)+(1*4)=186
186 % 10 = 6
So 99356-64-6 is a valid CAS Registry Number.

99356-64-6Downstream Products

99356-64-6Relevant academic research and scientific papers

Synthesis of 4-Hydroxy-N--2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-Dioxide and oxoacetic Acid. Major Metabolites of Isoxicam

Sircar, Jagadish C.,Capiris, Thomas,Bobovski, Thomas P.,Schwender, Charles F.

, p. 5723 - 5727 (1985)

4-Hydroxy-N--2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (2), the major oxidative human metabolite of isoxicam (1), and oxoacetic acid (3), the major rat metabolite of isoxicam (1), were synthesized. 2 was synthesized by condensation of the known benzothiazine ester 8 with the isoxazolamine 9b. 9b was synthesized via a nine-step sequence starting with 5-methyl-3-isoxazolecarboxylic acid (14).NBS bromination of 14 gave 5-(bromomethyl)-3-isoxazolecarboxylic acid, which was coverted to the carbamate ester via a Curtius rearrangement of the acid azide.Displacement of bromine with silver acetate gave the acetoxy compound 21.Hydrolysis of 21 gave the unstable 3-isoxazolamine derivative 9a, which was converted to the OSiMe3 derivative 9b.The compound 3 was synthesized by reaction of ethyl oxalyl chloride with 5-methyl-3-isoxazolamine followed by base hydrolysis.

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