136295-82-4 Usage
Uses
Used in Pharmaceutical Research:
3,5-Dimethyl-4-(2-nitrophenyl)isoxazole is used as a research compound for the development of new drugs for treating pain, inflammation, and neurodegenerative diseases due to its anti-inflammatory and analgesic properties.
Used in Organic Synthesis:
3,5-Dimethyl-4-(2-nitrophenyl)isoxazole is used as a building block in the synthesis of other organic compounds, contributing to the creation of various chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 136295-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,9 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136295-82:
(8*1)+(7*3)+(6*6)+(5*2)+(4*9)+(3*5)+(2*8)+(1*2)=144
144 % 10 = 4
So 136295-82-4 is a valid CAS Registry Number.
136295-82-4Relevant academic research and scientific papers
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.
