90253-22-8 Usage
Uses
Used in Pharmaceutical Industry:
4-cyclopentyl-1H-Pyrazole is used as a key intermediate in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with desired therapeutic properties. Its unique structure allows for the creation of molecules that can target specific enzymes or pathways involved in disease processes, offering potential treatments for various health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 4-cyclopentyl-1H-Pyrazole is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and protecting agricultural resources.
Used in Research and Development:
4-cyclopentyl-1H-Pyrazole is also employed in research and development activities, where it serves as a starting material for creating new compounds with specific properties. Scientists can manipulate its structure to explore its potential biological activities, such as enzyme inhibition, and evaluate its applicability in various fields, including medicine and agriculture.
Overall, 4-cyclopentyl-1H-Pyrazole's unique structure and properties make it a versatile compound with potential applications in both the pharmaceutical and agrochemical industries, as well as in research and development for the creation of novel compounds with desired characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 90253-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90253-22:
(7*9)+(6*0)+(5*2)+(4*5)+(3*3)+(2*2)+(1*2)=108
108 % 10 = 8
So 90253-22-8 is a valid CAS Registry Number.
90253-22-8Relevant academic research and scientific papers
Syntheses with Aliphatic Dialdehydes, XXXVIII. - Synthesis and Properties of Cycloalkylmalonaldehydes
Reichardt, Christian,Ferwanah, Abdel-Rahman,Pressler, Wilfried,Yun, Kyeong-Yeol
, p. 649 - 679 (2007/10/02)
Vilsmeier formylation of cycloalkyl-substituted enol ethers (7,14a - c,23) yields the cycloalkylmalonaldehydes 1 - 5 for the first time.In solution 1 - 5 exist in the (E)-s-(E) enol form as vinylogous carboxylic acids.The reaction of 1 - 5 with suitable electrophiles and nucleophiles leads to cycloalkyl-substituted open-chain (29,30), carbocyclic (31) as well as heterocyclic compounds (32-40) with peculiar properties due to the presence of the lipophilic cycloalkyl group.
