304665-45-0 Usage
Uses
Used in Pharmaceutical Development:
1H-Pyrazole-3-carboxylic acid, 1-methyl-, hydrazide (9CI) is used as a versatile building block in the synthesis of various heterocyclic compounds for pharmaceutical applications. Its diverse biological activities make it a promising candidate for the development of new drugs.
Used in Agrochemical Development:
In the agrochemical industry, 1H-Pyrazole-3-carboxylic acid, 1-methyl-, hydrazide (9CI) is used as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used as an Anti-tuberculosis Agent:
1H-Pyrazole-3-carboxylic acid, 1-methyl-, hydrazide (9CI) has been studied for its potential as an anti-tuberculosis agent, offering a promising avenue for the development of new treatments against this infectious disease.
Used as a Corrosion Inhibitor:
1H-Pyrazole-3-carboxylicacid,1-methyl-,hydrazide(9CI) has shown potential as a corrosion inhibitor, making it useful in various industrial applications where protection against metal corrosion is necessary.
Used in Cancer and Inflammation Treatment:
1H-Pyrazole-3-carboxylic acid, 1-methyl-, hydrazide (9CI) has been investigated for its potential use in the treatment of cancer and inflammation, highlighting its versatility in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 304665-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,6,6 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 304665-45:
(8*3)+(7*0)+(6*4)+(5*6)+(4*6)+(3*5)+(2*4)+(1*5)=130
130 % 10 = 0
So 304665-45-0 is a valid CAS Registry Number.
304665-45-0Relevant academic research and scientific papers
Narrow SAR in odorant sensing Orco receptor agonists
Romaine, Ian M.,Taylor, Robert W.,Saidu, Samsudeen P.,Kim, Kwangho,Sulikowski, Gary A.,Zwiebel, Laurence J.,Waterson, Alex G.
, p. 2613 - 2616 (2014/06/09)
The systematic exploration of a series of triazole-based agonists of the cation channel insect odorant receptor is reported. The structure-activity relationships of independent sections of the molecules are examined. Very small changes to the compound structure were found to exert a large impact on compound activity. Optimal substitutions were combined using a 'mix-and-match' strategy to produce best-in-class compounds that are capable of potently agonizing odorant receptor activity and may form the basis for the identification of a new mode of insect behavior modification.
