872407-85-7 Usage
Uses
Used in Pharmaceutical Industry:
3-(5-Amino-3-methyl-1H-pyrazol-1-yl)benzoic acid is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its versatile reactivity allows for the development of new drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
3-(5-Amino-3-methyl-1H-pyrazol-1-yl)benzoic acid is used as an intermediate in the production of agrochemicals. Its unique structural properties contribute to the development of effective agrochemical compounds for crop protection and pest control.
Used in Material Science:
3-(5-Amino-3-methyl-1H-pyrazol-1-yl)benzoic acid has potential applications in the development of new materials due to its unique structural properties. It can be utilized in the synthesis of advanced materials with specific properties for various industrial applications.
Used in Biomedical Research:
3-(5-Amino-3-methyl-1H-pyrazol-1-yl)benzoic acid is used in biomedical research for the exploration of its potential applications in drug discovery and development. Its unique chemical structure offers opportunities for the design and synthesis of novel bioactive compounds with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 872407-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,4,0 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 872407-85:
(8*8)+(7*7)+(6*2)+(5*4)+(4*0)+(3*7)+(2*8)+(1*5)=187
187 % 10 = 7
So 872407-85-7 is a valid CAS Registry Number.
872407-85-7Relevant academic research and scientific papers
One-pot, telescoped synthesis of N-aryl-5-aminopyrazoles from anilines in environmentally benign conditions
Marinozzi, Maura,Marcelli, Gloria,Carotti, Andrea,Natalini, Benedetto
, p. 7019 - 7023 (2014/02/14)
An efficient synthetic approach to synthesize N-aryl-5-aminopyrazoles from anilines via a one-pot, telescoped reaction performed in entirely aqueous conditions has been developed. This protocol provides a rapid, convenient method to prepare N-aryl-5-aminopyrazoles, useful building blocks for the synthesis of several bicyclic nitrogen heterocycles, by avoiding the isolation of the toxic intermediate arylhydrazines and the use of a metallic reductant. The Royal Society of Chemistry 2014.
