884502-25-4 Usage
Chemical structure
A 1,3-propanedione backbone with a 2-methoxy-3-pyridinyl group attached to one end and a 4-nitrophenyl group attached to the other.
Molecular weight
Approximately 247.21 g/mol
Appearance
It is likely a solid or crystalline substance, although the specific appearance is not provided in the material.
Research and pharmaceutical applications
Commonly used as a building block for the synthesis of other compounds.
Biological activity
Has potential biological activity and is currently being investigated for its potential use as an antifungal agent.
Enzyme and receptor inhibition
Has been studied for its potential to inhibit specific enzymes and receptors in the body, making it a promising candidate for further drug development.
Solubility
The solubility of 1,3-Propanedione, 1-(2-methoxy-3-pyridinyl)-3-(4-nitrophenyl)- is not mentioned in the material provided, but it may be soluble in organic solvents like ethanol or dimethyl sulfoxide (DMSO) due to its chemical structure.
Stability
The stability of the compound under various conditions (e.g., temperature, pH, light exposure) is not provided in the material, but it is generally important to consider when handling and storing chemical compounds.
Safety precautions
As with any chemical compound, it is essential to follow proper safety protocols when handling, storing, and using 1,3-Propanedione, 1-(2-methoxy-3-pyridinyl)-3-(4-nitrophenyl)-. This may include wearing appropriate personal protective equipment (PPE) and using proper containment and disposal methods.
Check Digit Verification of cas no
The CAS Registry Mumber 884502-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,5,0 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 884502-25:
(8*8)+(7*8)+(6*4)+(5*5)+(4*0)+(3*2)+(2*2)+(1*5)=184
184 % 10 = 4
So 884502-25-4 is a valid CAS Registry Number.
884502-25-4Relevant academic research and scientific papers
Synthesis of 2-aryl-4H-pyrano[2,3-b]pyridin-4-ones by a one-pot deprotection-cyclization reaction
Khlebnikov, Vladimir,Patel, Kalpesh,Zhou, Xiaojian,Reddy, M. Madhava,Su, Zhuoyi,Chiacchia, Fabrizio S.,Hansen, Henrik C.
experimental part, p. 6932 - 6940 (2009/12/06)
An efficient synthesis of 2-aryl-4H-pyrano[2,3-b]pyridine-4-ones is reported, using a one-pot, two step process in the presence of pyridinium hydrochloride. The methodology is compatible with a series of functional groups useful for the synthesis of secon
