structure of 2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

CAS No.: 1000577-84-3
M. Wt: 188.999
M. Fa: C6H2Cl2N2O
InChI Key: -

Names and Identifiers of 2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

CAS Number

1000577-84-3

IUPAC Name

2,4-bis(chloranyl)furo[2,3-d]pyrimidine

Canonical SMILES

C1=COC2=C1C(=NC(=N2)Cl)Cl

Physical and chemical properties of 2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

Acidity coefficient

-1.28±0.40(Predicted)

Density

1.6±0.1 g/cm3

Exact Mass

187.954422

Index of Refraction

1.646

LogP

2.17

Molecular Formula

C6H2Cl2N2O

Molecular Weight

188.999

PSA

38.92000

Safety Information of 2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

Pictograms

Signal Word

 Danger

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

The applications of 2,4-Dichlorofuro[2,3-D]pyrimidine extend primarily into medicinal chemistry. Its derivatives are being investigated for use as:

  • Anticancer Agents: Potential inhibitors of cancer cell growth.
  • Antimicrobial Agents: Compounds that may exhibit activity against various pathogens.
  • Pharmaceutical Intermediates: Useful in the synthesis of more complex pharmaceutical compounds due to their reactivity.

Interaction Studies of 2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

Interaction studies have focused on understanding how 2,4-Dichlorofuro[2,3-D]pyrimidine interacts with biological macromolecules. Preliminary studies suggest that it may bind to specific enzymes or receptors involved in cell signaling pathways related to cancer progression and microbial resistance. Further research is required to elucidate these interactions fully and assess their therapeutic implications.

Biological Activity of 2,4-DICHLOROFURO[2,3-D]PYRIMIDINE

Research indicates that 2,4-Dichlorofuro[2,3-D]pyrimidine exhibits notable biological activities, particularly in the realm of anticancer and antimicrobial properties. The compound's structure allows for interactions with biological targets, making it a candidate for further pharmacological studies. Its derivatives have shown promise in inhibiting specific enzymes related to cancer cell proliferation and microbial growth.