14633-22-8 Usage
General Description
3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID is a chemical compound with the molecular formula C7H9NO3. It is an isoxazole derivative with a carboxylic acid functional group at the 5-position and an isopropyl group at the 3-position. 3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is known for its antimicrobial and pesticidal properties, making it useful as a key intermediate in the development of various biologically active molecules. Additionally, 3-ISOPROPYLISOXAZOLE-5-CARBOXYLIC ACID has potential applications in the field of medicinal chemistry and drug discovery due to its structural features and biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 14633-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,3 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14633-22:
(7*1)+(6*4)+(5*6)+(4*3)+(3*3)+(2*2)+(1*2)=88
88 % 10 = 8
So 14633-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3/c1-4(2)5-3-6(7(9)10)11-8-5/h3-4H,1-2H3,(H,9,10)
14633-22-8Relevant articles and documents
Structural hybridization of pyrrolidine-based T-type calcium channel inhibitors and exploration of their analgesic effects in a neuropathic pain model
Son, Woo Seung,Jeong, Kyu-Sung,Lim, Sang Min,Pae, Ae Nim
, p. 1168 - 1172 (2019)
Highly effective and safe drugs for the treatment of neuropathic pain are urgently required and it was shown that blocking T-type calcium channels can be a promising strategy for drug development for neuropathic pain. We have developed pyrrolidine-based T
Ramoplanin derivatives possessing antibacterial activity
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Page/Page column 39; 50, (2010/11/23)
Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.
