CAS 13618-91-2

4,5,6,7-Tetrahydro-1H-indole

Description:

4,5,6,7-Tetrahydro-1H-indole is a bicyclic organic compound characterized by its saturated indole structure, which consists of a five-membered nitrogen-containing ring fused to a six-membered carbon ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to interact with various biological targets. The presence of the nitrogen atom in the ring contributes to its basicity and reactivity, making it a versatile building block in organic synthesis. Additionally, 4,5,6,7-Tetrahydro-1H-indole may exhibit interesting pharmacological properties, including effects on the central nervous system. Its solubility in organic solvents and relatively low molecular weight facilitate its use in various chemical reactions and formulations. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₈H₁₁N

InChI: InChI=1S/C8H11N/c1-2-4-8-7(3-1)5-6-9-8/h5-6,9H,1-4H2

InChI key: InChIKey=KQBVVLOYXDVATK-UHFFFAOYSA-N

SMILES: C12=C(NC=C1)CCCC2

Synonyms:

• 1H-Indole, 4,5,6,7-tetrahydro-
• 2,3-Tetramethylenepyrrole
• 4,5,6,7-Tetrahydro-1H-indole
• Cyclohex[b]pyrrole
• Indole, 4,5,6,7-tetrahydro-
• NSC 122455

4,5,6,7-Tetrahydroindole

CAS: 13618-91-2

Formula: C₈H₁₁N

Purity: 97%

Color and Shape: Solid

Molecular weight: 121.1796

Ref: IN-DA009BDU

4,5,6,7-Tetrahydro-1H-indole

CAS: 13618-91-2

4,5,6,7-Tetrahydro-1H-indole

Formula: C₈H₁₁N

Purity: 99%

Color and Shape: light red solid

Molecular weight: 121.18g/mol

Ref: 54-OR350389

4,5,6,7-Tetrahydro-1H-indole

CAS: 13618-91-2

Formula: C₈H₁₁N

Purity: 97%

Color and Shape: Solid

Molecular weight: 121.183

Ref: 10-F233782

4,5,6,7-Tetrahydro-1H-indole

CAS: 13618-91-2

4,5,6,7-Tetrahydro-1H-indole is a chemical compound that is an intermediate in the synthesis of other compounds. It reacts with halides to produce methyl sulfones and metal hydroxides. Tetrahydro-1H-indole can also react with acyl halides to form thiocyanates. The reaction mechanism has been studied using nmr spectra and chemical study. 4,5,6,7-Tetrahydro-1H-indole is an active substance that has been used in synthetic chemistry.

Formula: C₈H₁₁N

Purity: Min. 95%

Molecular weight: 121.18 g/mol

Ref: 3D-NAA61891