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5-bromo-2-(9-chloro-3-hydroxy-benzo[g]benzothiophen-2-yl)indol-3-one

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Identification
Molecular formula
C20H10BrClNO2S
CAS number
374913-74-3
IUPAC name
5-bromo-2-(9-chloro-3-hydroxy-benzo[g]benzothiophen-2-yl)indol-3-one
State
State

At room temperature, this compound is in a solid state. It is not soluble in water, but may dissolve in organic solvents.

Melting point (Celsius)
275.00
Melting point (Kelvin)
548.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
441.88g/mol
Molar mass
441.8750g/mol
Density
1.4900g/cm3
Appearence

This compound is typically a solid at room temperature and is often characterized by its crystalline form, appearing as a powder. The exact color can depend on the specific conditions and purity, but it generally has a grey or off-white appearance.

Comment on solubility

Solubility of 5-bromo-2-(9-chloro-3-hydroxy-benzo[g]benzothiophen-2-yl)indol-3-one

The solubility of 5-bromo-2-(9-chloro-3-hydroxy-benzo[g]benzothiophen-2-yl)indol-3-one can be influenced by various factors, making its study intriguing. Given its complex structure, the solubility characteristics include:

  • Polarity: The presence of halogen atoms (bromo and chloro) and hydroxyl (-OH) groups can increase polar interactions, potentially enhancing solubility in polar solvents.
  • Hydrogen bonding: The hydroxyl group may engage in hydrogen bonding, promoting solubility in protic solvents like water.
  • Nonpolar interactions: The aromatic and thiophenic components could lend the compound some solubility in nonpolar solvents.

As a result of these factors, one may observe a varied solubility profile depending on the solvent used:

  1. High solubility: Likely in polar protic solvents such as ethanol or methanol.
  2. Moderate solubility: Expected in mixed solvents that can interact both with the polar and nonpolar parts of the molecule.
  3. Low solubility: In apolar solvents like hexane, due to the resistance posed by the polar functional groups.

In summary, understanding the solubility of this compound is crucial for optimizing its applications in various chemical and pharmaceutical contexts. As always, *"solubility can be a key to unlocking the potential of complex molecular designs!"*

Interesting facts

Interesting Facts about 5-bromo-2-(9-chloro-3-hydroxy-benzo[g]benzothiophen-2-yl)indol-3-one

This complex compound, known as 5-bromo-2-(9-chloro-3-hydroxy-benzo[g]benzothiophen-2-yl)indol-3-one, brings together an array of fascinating chemical features that underscore its significance in scientific research.

Chemical Structure & Composition

The structure of this compound showcases a rich interplay of heterocyclic compounds. It includes:

  • Indole core: A fundamental structure in many natural products and pharmaceuticals.
  • Benzothiophene ring: Contributes to its unique electronic properties and can enhance biological activity.
  • Chloro and bromo substituents: These halogens can play crucial roles in modulation of reactivity and interaction with biological targets.

Biological Significance

This compound is of great interest due to its potential biological activities. For instance:

  • Studies suggest that compounds similar in structure can exhibit anticancer properties.
  • Its unique arrangement may influence cell signaling pathways, making it a candidate for medicinal chemistry.

Applications & Research Directions

In the realm of synthetic organic chemistry, the synthesis of such compounds opens up new pathways for:

  • **Drug Development**: Its complex structure may lead to the discovery of new therapeutic agents.
  • **Chemical Biology**: Understanding how such compounds interact with biomolecules can provide insight into disease mechanisms.

In conclusion, 5-bromo-2-(9-chloro-3-hydroxy-benzo[g]benzothiophen-2-yl)indol-3-one encapsulates an intriguing synthesis of structure, reactivity, and potential applications that make it a noteworthy subject of ongoing research and exploration in the field of chemistry.

Synonyms
Vat Black 1
Helanthrene Black BL
Thioindigo Black
3687-67-0
Tina printing Black BL
Tina Grey BL
Nako Fast Grey BL
Solanthrene Grey BL
C.I. Vat Black 1
Solanthrene Printing Black BL
1328-19-4
Durindone Printing Black BL
Indanthrene Printing Black BL
Paradone Printing Black BLSF
Paradone Printing Black TLSF
Solanthrene Printing Black TL
Solanthrene Printing Black BLN
Solanthrene Printing Black TLN
3H-Indol-3-one, 5-bromo-2-(9-chloro-3-oxonaphtho[1,2-b]thien-2(3H)-ylidene)-1,2-dihydro-
EINECS 222-983-7
BRN 1169312
C.I. 73670
DTXSID2063135
3H-Indol-3-one, 5-bromo-2-(9-chloro-3-oxonaphtho(1,2-b)thien-2(3H)-ylidene)-1,2-dihydro-
5-bromo-2-(9-chloro-3-oxonaphtho[1,2-b]thien-2(3H)-ylidene)-1,2-dihydro-3H-indol-3-one
3-INDOLINONE, 5-BROMO-2-(9-CHLORO-3-OXONAPHTHO(1,2-b)THIEN-2(3H)-YLIDENE)-
5-Bromo-2-(9-chloro-3-oxonaphtho(1,2-b)thien-2(3H)-ylidene)-1,2-dihydro-3H-indol-3-one
C.I. Vat Black 16
DTXCID8039247
DTXSID501057758
222-983-7
603-667-1
Vat Black 16
5-bromo-2-(9-chloro-3-hydroxybenzo[g][1]benzothiol-2-yl)indol-3-one
(2E)-5-bromo-2-(9-chloro-3-oxobenzo[g][1]benzothiol-2-ylidene)-1H-indol-3-one
MJURASYNFLAELQ-UHFFFAOYSA-N
WRSWXNQFTKCPHT-UHFFFAOYSA-N
AKOS000592663
NS00020642
AG-690/36758045