956191-91-6 Usage
Molecular structure
2-(5-amino-1-phenyl-1H-pyrazol-4-ylcarbonylamino)acetic acid consists of a pyrazole ring with a phenyl group and an amino group attached to it, along with a carboxylic acid and an amide group.
Amino acid derivative
It is an amino acid derivative due to the presence of the carboxylic acid and amide groups in its structure.
Potential applications
This chemical compound has potential applications in medicinal chemistry and drug development.
Biological activity
The compound may exhibit biological activity due to its structural features, making it a potential candidate for further research and development.
Building block for new pharmaceutical drugs
It could potentially be used as a building block for synthesizing new pharmaceutical drugs, contributing to the creation of innovative treatments and medications.
Research tool
2-(5-amino-1-phenyl-1H-pyrazol-4-ylcarbonylamino)acetic acid can serve as a research tool in studying the structure-activity relationships of similar compounds, aiding in the understanding of how these compounds interact with biological systems.
Further research
Additional research may reveal the specific properties and potential uses of this chemical compound, expanding its potential applications and contributions to the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 956191-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,1,9 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 956191-91:
(8*9)+(7*5)+(6*6)+(5*1)+(4*9)+(3*1)+(2*9)+(1*1)=206
206 % 10 = 6
So 956191-91-6 is a valid CAS Registry Number.
956191-91-6Relevant academic research and scientific papers
Synthesis of new di-, tetra-, and hexahydropyrazolo[3,4-e][1,4]diazepine derivatives
Bol'But,Kemskii,Vovk
, p. 991 - 1002 (2012/11/07)
Alkaline hydrolysis of 5-(2,2-diethoxyethyl-, aroylmethyl-, or ethoxycarbonylmethyl)-1H-pyrazolo-[3,4-e]pyrimidin-4(5H)-ones gave 5-amino-N-(2,2-diethoxyethyl-, aroylmethyl-, or carboxymethyl)-1H-pyrazole-4- carboxamides which underwent cyclization to the
