443107-13-9

Basic information

• Product Name: 5-amino-1-(2-phenylethyl)-1H-pyrazole-4-carboxylic acid(SALTDATA: FREE)
• Synonyms: 5-amino-1-(2-phenylethyl)-1H-pyrazole-4-carboxylic acid(SALTDATA: FREE);5-AMINO-1-PHENETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID
• CAS NO: 443107-13-9
• Molecular Formula: C₁₂H₁₃N₃O₂
• Molecular Weight: 231.25052
• Mol File: 443107-13-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-amino-1-(2-phenylethyl)-1H-pyrazole-4-carboxylic acid(SALTDATA: FREE)(CAS DataBase Reference)
• NIST Chemistry Reference: 5-amino-1-(2-phenylethyl)-1H-pyrazole-4-carboxylic acid(SALTDATA: FREE)(443107-13-9)
• EPA Substance Registry System: 5-amino-1-(2-phenylethyl)-1H-pyrazole-4-carboxylic acid(SALTDATA: FREE)(443107-13-9)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 443107-13-9(Hazardous Substances Data)

Upstream product

• 159979-74-5 5-amino-4-cyano-1-(β-phenylethyl)pyrazole 

Downstream Products

• 443107-17-3 C₁₃H₁₂N₄O₂ 
• 443107-17-3 6-Hydroxy-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ol 

Relevant articles and documents

Antagonists of the human adenosine A2A receptor. Part 3: Design and synthesis of pyrazolo[3,4-d]pyrimidines, pyrrolo[2,3-d]pyrimidines and 6-arylpurines

A series of pyrazolo[3,4-d]pyrimidine, pyrrolo[2,3-d]pyrimidine and 6-arylpurine adenosine A2A antagonists is described. Many examples were highly selective against the human A1 receptor sub-type and were active in an in vivo model of Parkinson's disease.