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CAS 89392-03-0

:

Carbamic acid, N-(4,6-dimethoxy-2-pyrimidinyl)-, phenyl ester

Description:
Carbamic acid, N-(4,6-dimethoxy-2-pyrimidinyl)-, phenyl ester, with the CAS number 89392-03-0, is an organic compound characterized by its carbamate functional group. This substance features a pyrimidine ring substituted with two methoxy groups at the 4 and 6 positions, which contributes to its chemical reactivity and potential biological activity. The phenyl ester moiety enhances its lipophilicity, potentially affecting its solubility and permeability in biological systems. Typically, compounds of this nature may exhibit pharmacological properties, making them of interest in medicinal chemistry. The presence of the pyrimidine structure suggests potential interactions with biological targets, such as enzymes or receptors. Additionally, the methoxy groups can influence the compound's electronic properties and steric hindrance, which may affect its binding affinity and selectivity. Overall, this compound's unique structural features position it as a candidate for further investigation in drug development or agricultural applications, depending on its specific activity profile.
Formula:C13H13N3O4
InChI:InChI=1/C13H13N3O4/c1-18-10-8-11(19-2)15-12(14-10)16-13(17)20-9-6-4-3-5-7-9/h3-8H,1-2H3,(H,14,15,16,17)
InChI key:InChIKey=MESPVSMSORHLAX-UHFFFAOYSA-N
SMILES:N(C(OC1=CC=CC=C1)=O)C=2N=C(OC)C=C(OC)N2
Synonyms:
  • (4,6-Dimethoxy-Pyrimidin-2-Yl)-Carbamic Acid Phenyl Ester
  • 2-((Phenoxycarbonyl)Amino)-4,6-Dimethoxypyrimidine
  • 2-Phenoxycarbonylamino-4,6-dimethoxypyrimidine
  • 4,6-Dimethoxy-2-(phenoxycarbonylamino)-pyrimidine
  • 4,6-dimethoxy-N-phenyl-2-pyrimidinamine
  • Carbamic acid, (4,6-dimethoxy-2-pyrimidinyl)-, phenyl ester
  • Carbamic acid, N-(4,6-dimethoxy-2-pyrimidinyl)-, phenyl ester
  • N-(4,6-Dimethoxypyrimidin-2-yl)carbamic acid phenyl ester
  • Phenyl (4,6-Dimethoxypyrimidin-2-Yl)Carbamate
  • Phenyl(4,6-dimethoxy-2-pyrimidinyl)carbamate
  • See more synonyms
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