Interesting facts
Interesting Facts about 1H-indole-5-carbonitrile
1H-indole-5-carbonitrile is a fascinating compound that belongs to the class of indole derivatives. Here are some intriguing aspects worth noting:
- Chemical Structure: This compound features an indole ring, which is a bicyclic structure composed of a benzene ring fused to a pyrrole ring. This unique arrangement is the foundation for many naturally occurring compounds and is known for its aromatic properties.
- Biological Significance: Indole derivatives have garnered considerable attention in medicinal chemistry due to their presence in the structure of various natural products. They are often associated with biological activities, including antimicrobial, anticancer, and anti-inflammatory effects.
- Versatile Applications: 1H-indole-5-carbonitrile serves as a valuable building block in organic synthesis. It is particularly useful in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Its utility stems from the ability to modify its structure, leading to a plethora of compounds with varying biological and chemical properties.
- Research Interest: The study of 1H-indole-5-carbonitrile continues to thrive in the scientific community. Researchers are actively exploring its role in drug discovery, as the indole scaffold is a common motif in many bioactive compounds.
- Synthetic Methodologies: There are various synthetic approaches for the preparation of 1H-indole-5-carbonitrile. Methods may include cyclization reactions, and those based on starting materials such as anilines and ketones, showcasing the compound’s versatility in synthesis.
In summary, 1H-indole-5-carbonitrile is more than just a chemical structure; it represents a connection to the rich world of organic chemistry and its applications in health and agriculture. The compound exemplifies how a seemingly simple molecule can lead to significant advancements in various fields.
Synonyms
5-Cyanoindole
1H-Indole-5-carbonitrile
INDOLE-5-CARBONITRILE
EINECS 239-986-4
DTXSID40166477
DTXCID5088968
239-986-4
InChI=1/C9H6N2/c10-6-7-1-2-9-8(5-7)3-4-11-9/h1-5,11
YHYLDEVWYOFIJK-UHFFFAOYSA-N
15861-24-2
5-Cyano-1H-indole
MFCD00005669
5-Indolecarbonitrile
CHEMBL294926
5-Cyano indole
5-cyano-indole
indol-5-carbonitrile
Indole, 5-cyano-
SCHEMBL91366
Indole-5-carbonitrile, 99%
orb2941102
SCHEMBL1092139
SCHEMBL2072467
SCHEMBL5949367
SCHEMBL30389000
ALBB-022905
BCP26499
CS-M1444
STR04400
BDBM50220678
SBB004148
STK802138
AKOS005206715
AC-7424
CG-0514
FC00158
PB25883
SB20070
NCGC00340972-01
240812-99-1
BP-10151
HY-77057
SY006206
DB-014571
NS00025158
ST50823781
EN300-97267
AB01331743-02
F2158-0363
Z1203730728
A3327A31-2A0C-4860-8157-F2773DE25B9E
91201-84-2
Solubility of 1H-Indole-5-carbonitrile
1H-Indole-5-carbonitrile, with the chemical formula C9H6N2, exhibits interesting solubility characteristics that are important for its applications in various chemical processes.
Solubility Characteristics
The solubility of 1H-indole-5-carbonitrile can be influenced by several factors:
In summary, the solubility of 1H-indole-5-carbonitrile can be categorized as moderate, which is often suitable for various synthetic and analytical applications. However, it is essential to choose the appropriate solvent and conditions to achieve optimal solubility. As a guideline:
Understanding the solubility of this compound is crucial for researchers looking to work with it effectively in both laboratory and industrial settings.