1021950-41-3 Usage
Molecular structure
1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-[(4-nitrophenyl)amino]-, ethyl ester has a complex structure consisting of a pyrrolopyridine core, a carboxylic acid group at one end, and an ethyl ester group at the other end. The molecule also contains a 4-[(4-nitrophenyl)amino] moiety, which is a nitrophenyl group linked to an amino group.
Chemical classification
This compound is classified as an ester, specifically an ethyl ester, due to the presence of the ethoxy group (-OCH2CH3) in its structure.
Aromaticity
The pyrrolopyridine core and the nitrophenyl group in the molecule contribute to its aromatic character, which may influence its chemical reactivity and stability.
Functional groups
The presence of the carboxylic acid (-COOH) and amino (-NH2) functional groups suggests that this compound may exhibit acidic and basic properties, respectively.
Solubility
The compound may have varying solubility in different solvents, such as polar solvents (e.g., water, methanol) due to the presence of the carboxylic acid and amino groups, and nonpolar solvents (e.g., hexane, toluene) due to the ethyl ester group.
Reactivity
The compound may undergo various chemical reactions, such as ester hydrolysis, amide formation, and nitro group reduction, depending on the reaction conditions and the presence of appropriate reagents.
Potential applications
1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-[(4-nitrophenyl)amino]-, ethyl ester may have potential uses in pharmaceutical research, materials science, or other industrial applications, depending on its specific properties and characteristics.
Stability
The compound's stability may be influenced by factors such as temperature, pH, and the presence of other chemicals or catalysts. Proper storage and handling conditions should be considered to maintain its stability.
Synthesis
The synthesis of this compound may involve multiple steps, including the formation of the pyrrolopyridine core, the introduction of the carboxylic acid and ethyl ester groups, and the attachment of the 4-[(4-nitrophenyl)amino] moiety. The specific synthetic route and conditions would depend on the desired yield and purity of the final product.
Analytical techniques
Various analytical techniques, such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and infrared (IR) spectroscopy, can be used to characterize and confirm the structure of 1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-[(4-nitrophenyl)amino]-, ethyl ester.
Check Digit Verification of cas no
The CAS Registry Mumber 1021950-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,9,5 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1021950-41:
(9*1)+(8*0)+(7*2)+(6*1)+(5*9)+(4*5)+(3*0)+(2*4)+(1*1)=103
103 % 10 = 3
So 1021950-41-3 is a valid CAS Registry Number.
1021950-41-3Relevant articles and documents
NOVEL COMPOUNDS
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Page/Page column 54-55, (2008/12/05)
The present invention relates to compounds of formula (I): and processes for preparing them, compositions containing them and their use in treating diseases relating to inappropriate c-Met activity.
