13627-02-6 Usage
Uses
Used in Pharmaceutical Synthesis:
5-METHYLOXAZOL-2-OL is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse therapeutic applications.
Used in Antimicrobial Agents Development:
Leveraging its antimicrobial properties, 5-METHYLOXAZOL-2-OL is utilized as a starting material in the development of new antimicrobial agents. This is particularly important in the face of increasing antibiotic resistance and the need for novel treatments.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-METHYLOXAZOL-2-OL is employed as a component in the design and development of new drugs and therapeutic agents. Its structural attributes make it a valuable asset in creating molecules with specific biological activities and therapeutic potentials.
Check Digit Verification of cas no
The CAS Registry Mumber 13627-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,2 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13627-02:
(7*1)+(6*3)+(5*6)+(4*2)+(3*7)+(2*0)+(1*2)=86
86 % 10 = 6
So 13627-02-6 is a valid CAS Registry Number.
13627-02-6Relevant articles and documents
Photolysis of 3 hydroxyisoxazoles
Nakagawa,Nakamura,Tomita
, p. 2205 - 2208 (1974)
Photolysis of 3 hydroxy 5 phenylisoxazole in methanol with a low pressure mercury lamp afforded 5 phenyl 4 oxazolin 2 one, together with small amounts of benzoic acid and benzoylacetamide. Similarly, 3 hydroxy 5 methylisoxazole in distilled water afforded 5 methyl 4 oxazolin 2 one as the major product. Both isoxazoles were stable in sunlight for up to 20 days.
A NEW VERSATILE SYNTHESIS OF 4-ACYL-5-METHYL-4-ISOXAZOLIN-3-ONES
Sugai, Soji,Sato, Kazuo,Ueda, Takashi,Kataoka, Kumiko,Tomita, Kazuo
, p. 1123 - 1126 (2007/10/02)
Treatment of N-substituted N-hydroxyacetoacetamides 1 with acyl chlorides in the presence of two equivalents of triethylamine gave 4-acyl-5-methyl-4-isoxazolin-3-ones 5.The reaction was thought to proceed via acyl rearrangement as shown in 8 and 9.
