Ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate, also known as Ethyl 1-(2-nitrophenyl)-5-aminopyrazole-4-carboxylate, is a chemical compound belonging to the class of pyrazole derivatives. It is characterized by the presence of an ethyl ester group, an amino group, and a nitrophenyl group attached to a pyrazole ring. ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate has potential applications in pharmaceutical research and development due to its diverse biological activities and the unique combination of functional groups.
16459-33-9
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Basic information
- Product Name: ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate
- Synonyms: ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate;5-Amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylic acid ethyl ester
- CAS NO:16459-33-9
- Molecular Formula: C12H12N4O4
- Molecular Weight: 276.24808
- EINECS: N/A
- Product Categories: N/A
- Mol File: 16459-33-9.mol
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Chemical Properties
- Melting Point: 115-116℃
- Boiling Point: 464.195 °C at 760 mmHg
- Flash Point: 234.537 °C
- Appearance: /
- Density: 1.45
- Refractive Index: N/A
- Storage Temp.: 2-8°C
- Solubility: N/A
- PKA: 0.17±0.13(Predicted)
- CAS DataBase Reference: ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate(CAS DataBase Reference)
- NIST Chemistry Reference: ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate(16459-33-9)
- EPA Substance Registry System: ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate(16459-33-9)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 16459-33-9(Hazardous Substances Data)
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16459-33-9 Usage
Uses
Used in Pharmaceutical Research and Development:Ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate is used as a potential drug candidate or pharmacological tool in the pharmaceutical industry. Its unique structure and functional groups make it an interesting compound for medicinal chemists and pharmacologists studying the development of new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate is used for the synthesis and investigation of its properties. The presence of the ethyl ester, amino, and nitrophenyl groups attached to the pyrazole ring allows for further modification and exploration of its potential therapeutic applications.
Used in Drug Discovery:
Ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate is utilized in drug discovery processes to identify novel therapeutic agents with potential biological activities. Its diverse functional groups provide opportunities for optimization and the development of new drug candidates with improved efficacy and selectivity.
Used in Pharmacology:
In pharmacology, ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate is employed for studying its interactions with biological targets and understanding its mechanism of action. This knowledge can contribute to the development of more effective and safer drugs for various therapeutic applications.
Used in Chemical Synthesis:
Ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate is used as a starting material or intermediate in the synthesis of other pyrazole-based compounds with potential pharmaceutical applications. Its versatile structure allows for the introduction of various functional groups and modifications to explore new chemical entities with improved properties.
Check Digit Verification of cas no
The CAS Registry Mumber 16459-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,5 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.Calculate Digit Verification of CAS Registry Number 16459-33:
(7*1)+(6*6)+(5*4)+(4*5)+(3*9)+(2*3)+(1*3)=119
119 % 10 = 9
So 16459-33-9 is a valid CAS Registry Number.
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ethyl 5-amino-1-(2-nitrophenyl)-1H-pyrazole-4-carboxylate
