CAS 21017-47-0
:3-(Phenylamino)propanamide
Description:
3-(Phenylamino)propanamide, with the CAS number 21017-47-0, is an organic compound characterized by the presence of an amide functional group and a phenylamino substituent. This compound features a three-carbon propanamide backbone, where one of the carbons is bonded to a phenyl group through an amino linkage. The presence of the phenyl group contributes to its aromatic characteristics, potentially influencing its solubility and reactivity. Typically, amides exhibit moderate polarity due to the carbonyl group, which can engage in hydrogen bonding, affecting their boiling and melting points. The compound may be used in various chemical syntheses or as an intermediate in pharmaceutical applications, given the importance of amide functionalities in medicinal chemistry. Its structural features suggest potential interactions with biological systems, making it of interest in drug development. However, specific physical and chemical properties such as melting point, boiling point, and solubility would need to be referenced from experimental data or literature for precise applications.
Formula:C9H12N2O
InChI:InChI=1S/C9H12N2O/c10-9(12)6-7-11-8-4-2-1-3-5-8/h1-5,11H,6-7H2,(H2,10,12)
InChI key:InChIKey=BNXCBLMAWSXTKD-UHFFFAOYSA-N
SMILES:N(CCC(N)=O)C1=CC=CC=C1
Synonyms:- 3-(Phenylamino)propanamide
- 3-Anilinopropanamide
- Propanamide, 3-(phenylamino)-
- Propionamide, 3-anilino-
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Found 2 products.
3-(Phenylamino)propanamide
CAS:<p>3-(Phenylamino)propanamide is an alkali agent that is used to hydrolyze esters and dihydrouracils. 3-(Phenylamino)propanamide is a potent inhibitor of the enzyme uracil-DNA glycosylase, which repairs DNA damage caused by UV light or other forms of radiation. This drug also inhibits the enzyme DNA polymerase, which is needed to replicate damaged DNA. The inhibition of these enzymes leads to cell death.</p>Formula:C9H12N2OPurity:Min. 95%Molecular weight:164.2 g/mol
