CAS 14465-74-8

PHENYL-PROP-2-YNYL-AMINE

Description:

Phenyl-prop-2-ynyl-amine, with the CAS number 14465-74-8, is an organic compound characterized by its structure, which includes a phenyl group attached to a prop-2-ynyl amine moiety. This compound features a triple bond in the prop-2-ynyl group, contributing to its reactivity and potential applications in organic synthesis. The presence of the amine functional group indicates that it can participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions. Phenyl-prop-2-ynyl-amine may exhibit properties typical of alkynes, including unique spectroscopic characteristics, such as distinct infrared absorption bands due to the C≡C bond. Additionally, its solubility and stability can vary depending on the solvent and environmental conditions. This compound may be of interest in medicinal chemistry and materials science due to its potential as a building block for more complex molecules. However, specific safety and handling guidelines should be followed, as with any chemical substance, to mitigate risks associated with its use.

Formula: C₉H₉N

InChI: InChI=1/C9H9N/c1-2-8-10-9-6-4-3-5-7-9/h1,3-7,10H,8H2

InChI key: IZKIWEYIOKPHLF-UHFFFAOYSA-N

SMILES: C#CCNc1ccccc1

Synonyms:

• Timtec-Bb Sbb010262
• N-(prop-2-yn-1-yl)aniline

N-Prop-2-ynylaniline

CAS: 14465-74-8

N-Prop-2-ynylaniline

Formula: C₉H₉N

Purity: ≥95%

Color and Shape: Liquid

Molecular weight: 131.17445

Ref: 54-OR54686

N-2-Propyn-1-ylbenzenamine

CAS: 14465-74-8

Formula: C₉H₉N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 131.1745

Ref: IN-DA001JXV

N-(Prop-2-yn-1-yl)aniline

CAS: 14465-74-8

N-(Prop-2-yn-1-yl)aniline

Formula: C₉H₉N

Purity: 95%

Molecular weight: 131.17

Ref: IN-DG147714

Phenyl-prop-2-ynyl-amine

CAS: 14465-74-8

Formula: C₉H₉N

Purity: 98%

Color and Shape: Liquid

Molecular weight: 131.178

Ref: 10-F043348

Phenyl-prop-2-ynyl-amine

CAS: 14465-74-8

Phenyl-prop-2-ynyl-amine is a primary amine with neuroprotective properties. It can be activated to the corresponding aniline by treatment with a base. Phenyl-prop-2-ynyl-amine has been shown to have neuroprotective effects in a model system of Parkinson's disease. It also possesses ring-opening activity on quinoline derivatives and gold nanoparticles. This reaction is slow, but it can be accelerated by the addition of a carboxylic acid. The use of this method for the synthesis of phenylpropene derivatives provides an efficient route for the construction of complex molecules with functional groups in their skeletons.

Formula: C₉H₉N

Purity: Min. 95%

Molecular weight: 131.17 g/mol

Ref: 3D-PAA46574