199682-74-1 Usage
Uses
Used in Organic Synthesis:
5-(2-CHLOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a wide range of molecules with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-(2-CHLOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is utilized as a building block for the development of new drugs. Its incorporation into molecular structures can lead to the discovery of novel therapeutic agents with improved pharmacological properties.
Used in Medicinal Chemistry:
5-(2-CHLOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is employed as a key component in the design and synthesis of biologically active molecules in medicinal chemistry. Its presence in a molecule can influence its interaction with biological targets, potentially leading to the development of new drugs with enhanced efficacy and selectivity.
Used in Drug Discovery:
In the realm of drug discovery, 5-(2-CHLOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE is used as a starting material for the exploration of new chemical entities. Its unique structural features make it a valuable asset in the search for innovative therapeutic agents that can address unmet medical needs.
While the specific applications of 5-(2-CHLOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE in various industries are still being explored, its role as a versatile building block in organic synthesis and pharmaceutical research is well-established. As research progresses, it is expected that the compound will find its place in an even broader range of applications, contributing to advancements in medicine and other related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 199682-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,6,8 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 199682-74:
(8*1)+(7*9)+(6*9)+(5*6)+(4*8)+(3*2)+(2*7)+(1*4)=211
211 % 10 = 1
So 199682-74-1 is a valid CAS Registry Number.
199682-74-1Relevant academic research and scientific papers
Synthesis and evaluation of antimicrobial and anticancer activities of 3-phenyl-1-phenylsulfonyl pyrazoles containing an aminoguanidine moiety
Huang, Yushan,Hu, Hongmei,Yan, Rui,Lin, Liwen,Song, Mingxia,Yao, Xiaodong
, (2020/10/15)
A series of 3-phenyl-1-phenylsulfonyl pyrazoles containing an aminoguanidine moiety was designed, synthesized, and evaluated for their antimicrobial and anticancer activities. The majority of the target compounds showed broad-spectrum antimicrobial activi
Synthesis and antimicrobial evaluation of (Z)-5-((3-phenyl-1H-pyrazol-4-yl)methylene)-2-thioxothiazolidin-4-one derivatives
Wei, Zhi-Yu,Liu, Jia-Chun,Zhang, Wen,Li, Ya-Ru,Li, Chao,Zheng, Chang-Ji,Piao, Hu-Ri
, p. 751 - 759 (2016/11/29)
Background: An alarming increment in pathogenic resistance to existing anti-microbial agents is a serious problem and the treatment of these bacterial infections is becoming increasingly challenging. Therefore, there is an urgent need to develop novel ant
A new synthethic approach to indazole synthesis
Baraldi, Pier Giovanni,Cacciari, Barbara,Spalluto, Giampiero,Romagnoli, Romeo,Braccioli, Giovanni,Zaid, Abdel Naser,De Pineda Las Infantas, Maria J.
, p. 1140 - 1142 (2007/10/03)
Stobbe condensation of 3-alkyl- or aryl-4-formylpyrazoles 3a-f with diethyl succinate in the presence of potassium f-butoxide, followed by intramolecular ring closure (Ac2O-NaOAc), afforded the corresponding indazole derivatives 5a-f in 65-85% overall yield. These compounds are good starting materials for transformation to biologically active molecules, such as new pyrazole analogs of the left-hand segment of the potent natural antineoplastic agent CC-1065.
