7064-38-2 Usage
Uses
Used in Organic Synthesis:
4-IODO-5-METHYL-ISOXAZOLE is used as a building block for the creation of various complex organic molecules. Its unique structure allows for the development of new compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-IODO-5-METHYL-ISOXAZOLE is utilized as a key intermediate in the synthesis of biologically active compounds. Its presence in these compounds can contribute to their pharmacological properties, making IMI a valuable component in drug discovery and development.
Used in Coordination Chemistry:
4-IODO-5-METHYL-ISOXAZOLE is used as a ligand in coordination chemistry, where it can bind to metal ions to form coordination compounds. These compounds have applications in areas such as catalysis, materials science, and medicinal chemistry.
Used in Catalysis:
As a component in catalytic systems, 4-IODO-5-METHYL-ISOXAZOLE can enhance the efficiency of chemical reactions. Its ability to act as a ligand allows it to stabilize and modulate the activity of catalysts, which is crucial in various industrial processes.
Used in Agrochemicals:
In the agrochemical industry, 4-IODO-5-METHYL-ISOXAZOLE is used as an intermediate for the synthesis of compounds with pesticidal or herbicidal properties. Its role in these applications contributes to the development of effective and targeted agrochemicals for crop protection.
Check Digit Verification of cas no
The CAS Registry Mumber 7064-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7064-38:
(6*7)+(5*0)+(4*6)+(3*4)+(2*3)+(1*8)=92
92 % 10 = 2
So 7064-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H4INO/c1-3-4(5)2-6-7-3/h2H,1H3
7064-38-2Relevant academic research and scientific papers
Enantioselective organo-SOMO cascade cycloadditions: A rapid approach to molecular complexity from simple aldehydes and olefins
Jui, Nathan T.,Lee, Esther C. Y.,MacMillan, David W. C.
supporting information; experimental part, p. 10015 - 10017 (2010/10/03)
A highly selective, radical-mediated (4 + 2) coupling reaction of aldehydes and conjugated olefins has been achieved through asymmetric SOMO-catalysis. A radical-polar crossover mechanism is proposed wherein olefin addition to a transient enamine radical cation and oxidation of the resulting radical furnishes a cation which is vulnerable to nucleophilic addition. A range of aromatic aldehydes are shown to couple with styrenes and dienes to provide cyclic products with high chemical efficiency, regioselectivity, and stereoselectivity.
