61292-63-5 Usage
Aromatic heterocyclic organic compound
It has a fused imidazole and benzene ring structure, which contributes to its aromatic properties and chemical reactivity.
Imidazole functional group
The presence of an imidazole ring in its structure makes it a versatile building block for the synthesis of various biologically active molecules.
Nitro group
The 5-position nitro group (-NO2) adds potential pharmacological activity and can influence the compound's reactivity and properties.
Pharmaceutical research and drug development
1H-Imidazole, 1-(2-methoxy-5-nitrophenyl)is commonly used as a building block for creating new drugs and biologically active molecules due to its unique structure and functional groups.
Biological activities
The compound has potential pharmacological activity due to the presence of both imidazole and nitro functional groups, which can lead to various biological effects.
Context-dependent properties
The specific properties and uses of 1H-Imidazole, 1-(2-methoxy-5-nitrophenyl)can vary depending on its chemical structure and the context in which it is used, such as different chemical reactions or biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 61292-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,9 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61292-63:
(7*6)+(6*1)+(5*2)+(4*9)+(3*2)+(2*6)+(1*3)=115
115 % 10 = 5
So 61292-63-5 is a valid CAS Registry Number.
61292-63-5Relevant articles and documents
The search for biochemical photoprobes. III. The photoreactions of 4-nitroveratrole and 2-fluoro-4-nitroanisole with bovine pancreatic ribonuclease A and with model nucleophiles
Marquet,Rafecas,Cantos,Moreno-Manas,Cervera,Casado,Nogues,Cuchillo
, p. 1297 - 1306 (1993)
The photoreactions of 4-nitroveratrole (NVT) and 2-fluoro-4-nitroanisole (FNA) with bovine pancreatic ribonuclease A (RNAase A) and with model nucleophiles are described. From them it is concluded that 2-fluoro-4-nitrophenyl ethers constitute improved alternative biochemical photoprobes, specially for proteins where a number of good nucleophiles are present.
