712-39-0 Usage
Uses
Used in Pharmaceutical Research and Development:
1-o-tolyl-1H-pyrazole-4-carbonitrile is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Organic Chemistry:
In the field of organic chemistry, 1-o-tolyl-1H-pyrazole-4-carbonitrile serves as a valuable compound for studying the reactivity and properties of pyrazole derivatives. Its carbonitrile functional group and tolyl substituent provide opportunities for further chemical modifications and exploration of novel reactions.
Used in Medicinal Chemistry:
1-o-tolyl-1H-pyrazole-4-carbonitrile is utilized as a key component in the design and synthesis of potential therapeutic agents. Its presence in a molecule can influence the pharmacokinetic and pharmacodynamic properties, making it an important factor in the optimization of drug candidates.
Used in Drug Discovery:
In the realm of drug discovery, 1-o-tolyl-1H-pyrazole-4-carbonitrile is employed as a starting material or a scaffold for the development of new pharmaceuticals. Its unique structural features can contribute to the discovery of innovative drugs with improved efficacy and selectivity for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 712-39-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 712-39:
(5*7)+(4*1)+(3*2)+(2*3)+(1*9)=60
60 % 10 = 0
So 712-39-0 is a valid CAS Registry Number.
712-39-0Relevant academic research and scientific papers
Unveiling Potent Photooxidation Behavior of Catalytic Photoreductants
Targos, Karina,Williams, Oliver P.,Wickens, Zachary K.
supporting information, p. 4125 - 4132 (2021/04/07)
We describe a photocatalytic system that reveals latent photooxidant behavior from one of the most reducing conventional photoredox catalysts, N-phenylphenothiazine (PTH). This aerobic photochemical reaction engages difficult to oxidize feedstocks, such as benzene, in C(sp2)-N coupling reactions through direct oxidation. Mechanistic studies are consistent with activation of PTH via photooxidation and with Lewis acid cocatalysts scavenging inhibitors inextricably formed in this process.
