126085-92-5 Usage
Uses
Used in Organic Synthesis:
5-Iodo-3-methyl-isoxazole is utilized as a building block in organic synthesis for its unique structural properties, allowing for the creation of diverse chemical entities.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 5-Iodo-3-methyl-isoxazole is considered for its potential therapeutic applications, given its ability to be incorporated into various drug molecules.
Used in Pesticide Development:
5-Iodo-3-methyl-isoxazole is used as a component in the development of pesticides due to its pesticidal properties, offering a new avenue for controlling pests in agriculture.
Used in Antimicrobial and Antifungal Agents:
5-Iodo-3-methyl-isoxazole is employed as an antimicrobial and antifungal agent, leveraging its biocidal activity to combat microbial infections.
Used in Agrochemicals:
5-Iodo-3-methyl-isoxazole is used as a potential precursor in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals.
Used in Materials Science:
In the field of materials science, 5-Iodo-3-methyl-isoxazole is explored for its potential to enhance or create new materials with specific properties, such as in the development of advanced polymers or other composites.
Check Digit Verification of cas no
The CAS Registry Mumber 126085-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,8 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126085-92:
(8*1)+(7*2)+(6*6)+(5*0)+(4*8)+(3*5)+(2*9)+(1*2)=125
125 % 10 = 5
So 126085-92-5 is a valid CAS Registry Number.
126085-92-5Relevant academic research and scientific papers
The synthesis of epiboxidine and related analogues as potential pharmacological agents
Kulu, Irem,Ocal, Nuket
scheme or table, p. 2054 - 2060 (2012/01/04)
Methyl epiboxidine-N-carboxylate (8) was synthesized from 7 under reductive Heck conditions (Scheme 2). The C-C coupling of the new epiboxidine analog 9 with aryl and heteroaryl halides gave by hydroarylation C-aryl, N-(3-methylisoxazol-5-yl)-substituted
Condensed heteroaromatic ring systems. XIX. Synthesis and reactions of 5-(tributylstannyl)isoxazoles
Sakamoto, Takao,Kondo, Yoshinori,Uchiyama, Daishi,Yamanaka, Hiroshi
, p. 5111 - 5118 (2007/10/02)
3-Substituted 5-(tributylstannyl)isoxazoles were newly synthesized by the 1,3-dipolar cyctoadditton of nitrile oxides to tributylethynylstannane. The iodination and the palladium-catalyzed benzoylation of 5-(tributylstannyl)-3-methylisoxazolegave 5-iodo-3-methylisoxazole and 3-methyl-5-isoxazolyl phenyl ketone in satisfactory yields, respectively. The palladium-catalyzed cross-coupling reaction of the stannylisoxazole with 2-bromonitrobenzene followed by the catalytic hydrogenation over Raney nickel resulted in the formation of 2-methyll-4(1H)-quinolinone in 57% overall yield.
SYNTHESIS AND REACTIONS OF 5-(TRIBUTYLSTANNYL)ISOXAZOLES
Kondo, Yoshinori,Uchiyama, Daishi,Sakamoto, Takao,Yamanaka, Hiroshi
, p. 4249 - 4250 (2007/10/02)
3-Substituted 5-(tributylstannyl)isoxazoles were synthesized in good yields by the 1,3-dipolar cycloaddition reaction of ethynyltributylstannane with nitrile oxides generated in situ. 3-Methyl-5-(tributylstannyl)isoxazole was easily converted to the corre
