400877-15-8 Usage
Uses
Used in Medicinal Chemistry:
1-(2-Chlorophenyl)-1H-pyrazole-4-carbaldehyde is used as a key intermediate in the synthesis of bioactive compounds for medicinal chemistry. Its unique structure allows for the creation of a variety of pharmaceutical agents that can target different biological pathways and diseases.
Used in Drug Synthesis:
In the pharmaceutical industry, 1-(2-chlorophenyl)-1H-pyrazole-4-carbaldehyde is used as a building block for the development of new drugs. Its versatility in chemical reactions enables the production of a range of therapeutic agents with potential applications in treating various medical conditions.
Used in Research and Development:
1-(2-Chlorophenyl)-1H-pyrazole-4-carbaldehyde is also utilized in research settings to explore its potential as a precursor for the creation of novel chemical entities. Its reactivity and structural features make it an interesting candidate for further investigation in the field of chemical biology and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 400877-15-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,8,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 400877-15:
(8*4)+(7*0)+(6*0)+(5*8)+(4*7)+(3*7)+(2*1)+(1*5)=128
128 % 10 = 8
So 400877-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H7ClN2O/c11-9-3-1-2-4-10(9)13-6-8(7-14)5-12-13/h1-7H
400877-15-8Relevant academic research and scientific papers
Electrophotocatalysis with a Trisaminocyclopropenium Radical Dication
Huang, He,Strater, Zack M.,Rauch, Michael,Shee, James,Sisto, Thomas J.,Nuckolls, Colin,Lambert, Tristan H.
supporting information, p. 13318 - 13322 (2019/08/12)
Visible-light photocatalysis and electrocatalysis are two powerful strategies for the promotion of chemical reactions. Here, these two modalities are combined in an electrophotocatalytic oxidation platform. This chemistry employs a trisaminocyclopropenium (TAC) ion catalyst, which is electrochemically oxidized to form a cyclopropenium radical dication intermediate. The radical dication undergoes photoexcitation with visible light to produce an excited-state species with oxidizing power (3.33 V vs. SCE) sufficient to oxidize benzene and halogenated benzenes via single-electron transfer (SET), resulting in C?H/N?H coupling with azoles. A rationale for the strongly oxidizing behavior of the photoexcited species is provided, while the stability of the catalyst is rationalized by a particular conformation of the cis-2,6-dimethylpiperidine moieties.
