304477-40-5 Usage
Uses
Used in Pharmaceutical Synthesis:
1-METHYL-3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE,97% is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form complex molecular structures that can exhibit therapeutic properties.
Used in Agrochemical Development:
In the agrochemical industry, 1-METHYL-3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE,97% serves as a building block in the creation of compounds that can be used in pest control and crop protection, leveraging its reactivity to form new agrochemical entities.
Used in Research and Development:
1-METHYL-3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE,97% is utilized as a reactant in research laboratories for the exploration of new chemical reactions and the development of novel organic compounds, underpinning scientific discovery and innovation in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 304477-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,4,7 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 304477-40:
(8*3)+(7*0)+(6*4)+(5*4)+(4*7)+(3*7)+(2*4)+(1*0)=125
125 % 10 = 5
So 304477-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O/c1-13-7-10(8-14)11(12-13)9-5-3-2-4-6-9/h2-8H,1H3
304477-40-5Relevant academic research and scientific papers
Synthesis and biological evaluation of some pyrazole derivatives, containing (Thio) semicarbazide, as dual anti-inflammatory antimicrobial agents
Liang, Zhaochang,Huang, Yuping,Wang, Shiben,Deng, Xianqing
, p. 1020 - 1030 (2019/10/28)
Background: Several series of pyrazole derivatives containing (thio) semicarbazide (4a-4h, 5a-5l, 6a-6f, 7a-7c) were designed and synthesized to screen dual inflammatory and antimicrobial activities. Methods: The products were characterized by1
Reactions of acetophenonmonomethyl- and -dimethylhydrazones with the Vilsmeier-Reagent; formation of pyrazol-4-carbiminium salts: A contribution to the mechanism
Brehme,Gruendemann,Schneider
, p. 700 - 706 (2007/10/03)
Kira discovered the formation of (4e) N,N-Dimethyl-N-[1,3-diphenylpyrazol-4-ylmethylen]ammonium perchlorat by the reaction from acetophenonphenylhydrazone 1e with the Vilsmeier-Reagent 2. On the example of the Acetophenonmonomethylhydrazone 1a we represen
