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CAS 2653-16-9

:

2-chloro-N-methyl-N-(4-nitrophenyl)acetamide

Description:
2-Chloro-N-methyl-N-(4-nitrophenyl)acetamide, with the CAS number 2653-16-9, is an organic compound characterized by its acetamide structure, which includes a chloro group and a nitrophenyl substituent. This compound typically appears as a solid at room temperature and is soluble in polar organic solvents. The presence of the nitro group contributes to its electron-withdrawing properties, influencing its reactivity and potential applications in organic synthesis. The chloro substituent can participate in nucleophilic substitution reactions, making this compound useful in various chemical transformations. Additionally, the methyl group attached to the nitrogen atom can affect the compound's steric and electronic properties, impacting its biological activity and interactions. Due to its structural features, 2-chloro-N-methyl-N-(4-nitrophenyl)acetamide may exhibit specific pharmacological properties, although detailed studies would be necessary to fully understand its biological implications. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or reactivity.
Formula:C9H9ClN2O3
InChI:InChI=1/C9H9ClN2O3/c1-11(9(13)6-10)7-2-4-8(5-3-7)12(14)15/h2-5H,6H2,1H3
InChI key:InChIKey=JAWLWNKATJAODJ-UHFFFAOYSA-N
SMILES:N(C(CCl)=O)(C)C1=CC=C(N(=O)=O)C=C1
Synonyms:
  • Acetanilide, 2-chloro-N-methyl-4′-nitro-
  • acetamide, 2-chloro-N-methyl-N-(4-nitrophenyl)-
  • α-Chloro-N-methyl-p-nitroacetanilide
  • 2-Chloro-N-methyl-N-(4-nitrophenyl)acetamide
  • Intedanib Impurity 11
  • Nintedanib-004
  • Nintedanib intermediate
  • 2-Chloro-N-methyl-4'-nitroacetanilide
  • Nintedanib impurity 3/2-Chloro-N-methyl-N-(4-nitrophenyl)acetamide
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