3399-56-2 Usage
Uses
Used in Pharmaceutical Synthesis:
5-Cyano-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a building block in the synthesis of various pharmaceutical compounds. Its versatile chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-Cyano-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a key intermediate for the synthesis of biologically active molecules. Its unique properties enable researchers to explore its potential in the development of new therapeutic agents.
Used in Drug Discovery:
5-Cyano-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester is utilized in drug discovery processes to identify and optimize compounds with desired pharmacological properties. Its potential biological activities make it a promising candidate for the development of new drugs.
Used in Anti-inflammatory Applications:
Due to its reported anti-inflammatory properties, 5-Cyano-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester is used as a therapeutic agent for the treatment of inflammation-related conditions. Its ability to modulate inflammatory pathways makes it a potential candidate for the development of anti-inflammatory drugs.
Used in Analgesic Applications:
5-Cyano-1-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester is also used as an analgesic agent for the management of pain. Its potential to alleviate pain through its pharmacological actions makes it a valuable tool in the development of pain relief medications.
Check Digit Verification of cas no
The CAS Registry Mumber 3399-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3399-56:
(6*3)+(5*3)+(4*9)+(3*9)+(2*5)+(1*6)=112
112 % 10 = 2
So 3399-56-2 is a valid CAS Registry Number.
3399-56-2Relevant academic research and scientific papers
Iodine-Catalyzed Regioselective Oxidative Cyclization of Aldehyde Hydrazones with Electron-Deficient Olefins for the Synthesis of Mefenpyr-Diethyl
Deng, Yun-Xia,Lin, Hao-Peng,Wang, Wen-Kang,Zhao, Sheng-Yin,Zheng, Jian,Zhu, Jia-Nan
, (2019/08/26)
A regioselective synthesis of polysubstituted dihydropyrazoles and pyrazoles through an iodine-catalyzed oxidative cyclization strategy of aldehyde hydrazones with electron-deficient olefins is described. The protocol adopts very mild reaction conditions and provides desirable yields. The reaction is supposed to proceed via a cascade C-H functionalization, C-N bond formation, and oxidation sequential processes. The overall simplicity and regioselectivity of the catalytic system make this approach a valuable and step-economical tool to construct a C-C bond for the synthesis of Mefenpyr-Diethyl.
CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF
-
, (2018/04/17)
Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.
A ONE STEP SYNTHESIS OF 4-CYANOPYRAZOLES
Hassaneen, Hamdi M.,Ead, Hamed A.,Elwan, Nehal M.,Shawali, Ahmed S.
, p. 2857 - 2862 (2007/10/02)
Reaction of nitrilimines 2 with fumaronitrile 6 yielded 4-cyanopyrazoles 8 in good yields.The structures of 8 were substantiated by comparison with their regioisomers 5-cyanopyrazoles 5, prepared by addition of 2 to acrylonitrile followed by oxidation of
