C15H11N3O3
281.27 g/mol
Research ReagentWarning
3-Amino-6-nitro-4-phenyl-1H-quinolin-2-one
CAS36020-93-6
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound
This compound is a nitrated quinolinone derivative containing an amino group and a phenyl substituent. It is primarily used as a laboratory reagent or research compound in chemical and pharmaceutical studies.
laboratory reagentresearch compound
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
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Referencesame scaffold
3-Amino-4-(2-chlorophenyl)-6-nitroquinolin-2(1H)-one
CAS55198-89-5
pharmaceutical intermediate
Referencesame scaffold
3-Amino-4-(2-chlorophenyl)-6-nitro-2(1H)-quinolinone
CAS1346604-43-0
pharmaceutical intermediate
Referencesame scaffold
STK380592
CAS5220-83-7
pharmaceutical intermediate
Referencesame scaffold
3-amino-6-chloro-1-methyl-4-phenylcarbostyril
CAS5220-02-0
pharmaceutical intermediate
Safety Reference
Warning
H302Harmful if swallowed
Identifiers
IUPAC Name
3-amino-6-nitro-4-phenyl-1H-quinolin-2-one
InChIKey
VBAGZJBCMMYDQZ-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)C2=C(C(=O)NC3=C2C=C(C=C3)[N+](=O)[O-])N
Synonyms (7)
- 3-Amino-6-nitro-4-phenylquinolin-2(1H)-one; Nitrazepam Imp. A (EP); Nitrazepam Impurity A
- Nitrazepam EP Impurity A
Sourcing 3-Amino-6-nitro-4-phenyl-1H-quinolin-2-one?
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