structure of 1-ACETYL-5-BROMO-7-CHLOROINDOLE

1-ACETYL-5-BROMO-7-CHLOROINDOLE

CAS No.: 1000343-44-1
M. Wt: 272.526
M. Fa: C10H7BrClNO
InChI Key: YWWFHTIPZJKUAY-UHFFFAOYSA-N

Names and Identifiers of 1-ACETYL-5-BROMO-7-CHLOROINDOLE

CAS Number

1000343-44-1

MDL Number

MFCD09880071

IUPAC Name

1-(5-bromo-7-chloro-1H-indol-1-yl)ethan-1-one

InChI

InChI=1S/C10H7BrClNO/c1-6(14)13-3-2-7-4-8(11)5-9(12)10(7)13/h2-5H,1H3

InChIKey

YWWFHTIPZJKUAY-UHFFFAOYSA-N

Canonical SMILES

CC(=O)N1C=CC2=CC(Br)=CC(Cl)=C21

UNSPSC Code

12352100

Physical and chemical properties of 1-ACETYL-5-BROMO-7-CHLOROINDOLE

Boiling Point

350.1±22.0 °C at 760 mmHg

Density

1.6±0.1 g/cm3

Exact Mass

270.939941

Flash Point

165.6±22.3 °C

H Bond Acceptors

1

H Bond Donors

0

Index of Refraction

1.649

LogP

3.50

Molecular Formula

C10H7BrClNO

Molecular Weight

272.526

PSA

22.00000

Storage condition

2-8°C

Vapour Pressure

0.0±0.8 mmHg at 25°C

Safety Information of 1-ACETYL-5-BROMO-7-CHLOROINDOLE

Pictograms

Signal Word

 Warning

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

Applications of 1-ACETYL-5-BROMO-7-CHLOROINDOLE

The applications of 1-(5-Bromo-7-chloro-1H-indol-1-yl)ethanone are diverse:

  • Research Tool: It serves as a valuable compound in biochemical research for studying enzyme interactions and cellular processes.
  • Potential Drug Development: Its biological activities suggest potential applications in drug development, particularly for anticancer therapies.

Interaction Studies of 1-ACETYL-5-BROMO-7-CHLOROINDOLE

Studies on the interactions of 1-(5-Bromo-7-chloro-1H-indol-1-yl)ethanone with various biomolecules have revealed significant insights into its mechanism of action:

  • Binding Studies: The compound has been shown to bind to specific enzymes and receptors, influencing their activity.
  • Temporal Effects: The stability and degradation of this compound over time can affect its long-term impact on cellular functions, highlighting the importance of studying its interactions under varying conditions.

Biological Activity of 1-ACETYL-5-BROMO-7-CHLOROINDOLE

The biological activity of 1-(5-Bromo-7-chloro-1H-indol-1-yl)ethanone has been a subject of interest due to its potential effects on various cellular processes:

  • Enzyme Inhibition: This compound has been shown to inhibit enzymes involved in cancer cell proliferation, suggesting its potential as an anticancer agent.
  • Cellular Effects: It influences cell signaling pathways, gene expression, and cellular metabolism, demonstrating its capability to affect different types of cells and their functions.
  • Molecular Mechanism: The compound interacts with specific biomolecules, leading to either inhibition or activation of their functions, which is crucial for understanding its therapeutic potential.