1H-Indole, 1-(2-propynyl)-, also known by its CAS number 19017-00-6, is an organic compound that features a bicyclic structure consisting of a fused benzene and pyrrole ring, characteristic of indole derivatives. This compound contains a propynyl group attached to the nitrogen atom of the indole ring, which influences its chemical reactivity and potential biological activity. Typically, indole derivatives are known for their diverse applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. The presence of the propynyl group can enhance the compound's lipophilicity and may affect its interaction with biological targets. In terms of physical properties, indole derivatives generally exhibit moderate to high melting and boiling points, and they may be soluble in organic solvents while being less soluble in water. The compound's reactivity can include electrophilic substitution reactions typical of indoles, making it a valuable building block in synthetic organic chemistry. Overall, 1H-Indole, 1-(2-propynyl)- represents a significant structure in the realm of medicinal chemistry and material science.

1H-Indole,1-(2-propynyl)-

19017-00-6: 1H-Indole, 1-(2-propynyl)-, also known by its CAS number 19017-00-6, is an organic compound that features a bicyclic structure consisting of a fused benzene and pyrrole ring, characteristic of indole derivatives. This compound contains a propynyl group attached to the nitrogen atom of the indole ring, which influences its chemical reactivity and potential biological activity. Typically, indole derivatives are known for their diverse applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. The presence of the propynyl group can enhance the compound's lipophilicity and may affect its interaction with biological targets. In terms of physical properties, indole derivatives generally exhibit moderate to high melting and boiling points, and they may be soluble in organic solvents while being less soluble in water. The compound's reactivity can include electrophilic substitution reactions typical of indoles, making it a valuable building block in synthetic organic chemistry. Overall, 1H-Indole, 1-(2-propynyl)- represents a significant structure in the realm of medicinal chemistry and material science.

1-(Prop-2-yn-1-yl)-1H-indole

<p>1-(Prop-2-yn-1-yl)-1H-indole is a n-alkyl indole that has been shown to catalyze the interphase.</p>

CAS 19017-00-6

1H-Indole,1-(2-propynyl)-

1-(Prop-2-yn-1-yl)-1H-indole

Ref: 54-OR1047088

1-(Prop-2-yn-1-yl)-1H-indole

Ref: 3D-UAA01700