N-(2-aminoethyl)-4,5-dibromo-1-methyl-1H-pyrrole-2-carboxamide
CAS No.:
1000933-11-8
M. Wt:
325.00
M. Fa:
C8H11Br2N3O
InChI Key:
CTPZYAIWMMFGQE-UHFFFAOYSA-N
Names and Identifiers of 1000933-11-8
CAS Number |
1000933-11-8 |
|---|---|
MDL Number |
MFCD09971454 |
IUPAC Name |
N-(2-aminoethyl)-4,5-dibromo-1-methylpyrrole-2-carboxamide |
InChI |
InChI=1S/C8H11Br2N3O/c1-13-6(4-5(9)7(13)10)8(14)12-3-2-11/h4H,2-3,11H2,1H3,(H,12,14) |
InChIKey |
CTPZYAIWMMFGQE-UHFFFAOYSA-N |
Canonical SMILES |
CN1C(=CC(=C1Br)Br)C(=O)NCCN |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000933-11-8
Acidity coefficient |
14.07±0.46(Predicted) |
|---|---|
Boiling Point |
415.4±45.0 °C(Predicted) |
Density |
1.94±0.1 g/cm3(Predicted) |
H Bond Acceptors |
2 |
H Bond Donors |
2 |
LogP |
0.712000413 |
Molecular Formula |
C8H11Br2N3O |
Molecular Weight |
325.00 |
Safety Information of 1000933-11-8
Applications of 1000933-11-8
N-(2-aminoethyl)-4,5-dibromo-1-methyl-1H-pyrrole-2-carboxamide has several notable applications:
- Proteomics Research: Due to its unique structure, it is utilized in studies related to protein interactions and modifications.
- Medicinal Chemistry: Potential development as an antimicrobial or anticancer agent.
- Chemical Biology: Used as a probe to study biological processes involving pyrrole derivatives.
These applications highlight its versatility and significance in scientific research.
Interaction Studies of 1000933-11-8
Interaction studies are crucial for understanding how N-(2-aminoethyl)-4,5-dibromo-1-methyl-1H-pyrrole-2-carboxamide interacts with biomolecules. Research indicates that this compound may bind to specific proteins or enzymes, potentially inhibiting their activity or altering their function. Techniques such as surface plasmon resonance or isothermal titration calorimetry can be employed to characterize these interactions quantitatively.