222541-76-6 Usage
Description
4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is a chemical compound with the molecular formula C9H6ClN3O2. It is a benzoyl chloride derivative that contains a 1,2,4-oxadiazole ring. 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is known for its versatility in organic synthesis and its potential applications in various fields due to its unique chemical structure.
Uses
Used in Pharmaceutical Industry:
4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is used as a reagent in organic synthesis for the production of pharmaceuticals and other fine chemicals. Its ability to participate in a wide range of chemical reactions makes it a valuable component in the development of new drugs and medicinal compounds.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is used as an active ingredient to combat various types of bacteria and other microorganisms. Its antimicrobial properties contribute to the development of new treatments and preventive measures against infections.
Used in Anticancer Applications:
4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is also used as a component in the development of anticancer agents. Its potential to exhibit anticancer properties makes it a promising candidate for further research and development in the field of oncology.
Used in Antifungal Applications:
In the realm of antifungal treatments, 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is utilized as a key component in the synthesis of compounds that target and inhibit fungal growth. This contributes to the creation of new antifungal medications and treatments.
Used in Dye and Pigment Industry:
4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is used as a versatile building block in the synthesis of dyes, pigments, and fluorescent compounds. Its ability to participate in various chemical reactions allows for the creation of a wide range of colorants and specialty chemicals for use in different industries.
Used in Fluorescent Compounds Synthesis:
In the field of fluorescent compounds, 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOYL CHLORIDE is used as a key component in the development of new fluorescent materials. These compounds have potential applications in various areas, including bioimaging, diagnostics, and sensing technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 222541-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,5,4 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 222541-76:
(8*2)+(7*2)+(6*2)+(5*5)+(4*4)+(3*1)+(2*7)+(1*6)=106
106 % 10 = 6
So 222541-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H7ClN2O2/c1-6-12-10(13-15-6)8-4-2-7(3-5-8)9(11)14/h2-5H,1H3
222541-76-6Relevant articles and documents
Palladium-Catalyzed Decarbonylative Difluoromethylation of Acid Chlorides at Room Temperature
Pan, Fei,Boursalian, Gregory B.,Ritter, Tobias
supporting information, p. 16871 - 16876 (2018/11/23)
Methods for the direct synthesis of difluoromethylated arenes are sparse, despite the importance of the difluoromethyl group in medical, agro-, and materials chemistry. A palladium-catalyzed decarbonylative cross-coupling reaction of acid chlorides with a difluoromethyl zinc reagent is achieved to access difluoromethylated compounds. The transformation proceeds at room temperature and shows broad functional group tolerance, thus providing a general and efficient method for decarbonylative difluoromethylation of a wide range of aromatic carboxylic acids.
