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1-(2-Chloro-benzyl)-1H-pyrazole-4-carboxylic acid is a chemical compound belonging to the pyrazole family, characterized by the presence of a carboxylic acid group and a chloro-benzyl moiety. This white solid has a molecular formula of C10H9ClN2O2 and is widely utilized in organic synthesis and medicinal chemistry as a key building block for the development of pharmaceuticals and agrochemicals. Its unique structural features, including the chloro-benzyl group, endow it with specific reactivity and properties, making it a valuable asset for a range of synthetic and scientific applications.

877977-33-8

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877977-33-8 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-Chloro-benzyl)-1H-pyrazole-4-carboxylic acid is used as a building block for the synthesis of various pharmaceuticals due to its unique reactivity and structural properties. The presence of the chloro-benzyl group allows for further functionalization and modification, enabling the creation of a diverse array of therapeutic compounds with potential applications in treating various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-Chloro-benzyl)-1H-pyrazole-4-carboxylic acid is employed as a starting material for the development of new agrochemicals. Its structural features and reactivity make it a suitable candidate for the synthesis of compounds with pesticidal, herbicidal, or fungicidal properties, contributing to the enhancement of crop protection and yield.
Used in Material Science:
1-(2-Chloro-benzyl)-1H-pyrazole-4-carboxylic acid also finds potential applications in the field of material science. Its unique properties and reactivity can be harnessed to develop novel materials with specific characteristics, such as improved mechanical strength, thermal stability, or chemical resistance, depending on the desired application.
Used in Chemical Research:
As a versatile chemical compound, 1-(2-Chloro-benzyl)-1H-pyrazole-4-carboxylic acid serves as a valuable tool for chemical research. It can be used to study various reaction mechanisms, explore new synthetic routes, and investigate the properties of related compounds, further expanding the understanding of the pyrazole family and its potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 877977-33-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,9,7 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 877977-33:
(8*8)+(7*7)+(6*7)+(5*9)+(4*7)+(3*7)+(2*3)+(1*3)=258
258 % 10 = 8
So 877977-33-8 is a valid CAS Registry Number.

877977-33-8Upstream product

877977-33-8Downstream Products

877977-33-8Relevant academic research and scientific papers

Design, synthesis, biological evaluation and in silico studies of pyrazole‐based nh2‐acyl oseltamivir analogues as potent neuraminidase inhibitors

Ye, Jiqing,Lin, Lin,Xu, Jinyi,Chan, Paul Kay-Sheung,Yang, Xiao,Ma, Cong

, (2021/05/05)

Oseltamivir represents one of the most successful neuraminidase (NA) inhibitors in the current anti‐influenza therapy. The 150‐cavity of NA was identified as an additional binding pocket, and novel NA inhibitors have been designed to occupy the 150‐cavity

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