19016-98-9

Basic information

• Product Name: 1H-Pyrrole, 1-(2-propynyl)-
• Synonyms: 1-(2-propynyl)pyrrole;N-propargylpyrrole;1-prop-2-ynyl-pyrrole;N-(prop-2-ynyl)pyrrole;1H-Pyrrole,1-(2-propynyl);1-(prop-2-yn-1-yl)-1H-pyrrole;1-Prop-2-inyl-pyrrol
• CAS NO: 19016-98-9
• Molecular Formula: C7H7N
• Molecular Weight: 105.139
• Mol File: 19016-98-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 70 °C(Press: 23 Torr)
• Density: 0.83±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1H-Pyrrole, 1-(2-propynyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole, 1-(2-propynyl)-(19016-98-9)
• EPA Substance Registry System: 1H-Pyrrole, 1-(2-propynyl)-(19016-98-9)

Safety Data

• Hazardous Substances Data: 19016-98-9(Hazardous Substances Data)

Upstream product

• 16199-06-7 potassium pyrrolide 
• 106-96-7 propargyl bromide 
• 109-97-7 pyrrole 

Downstream Products

• 139565-84-7 6-Pyrrol-1-yl-hexa-2,4-diyn-1-ol 

Relevant articles and documents

Iodonium-Induced Cyclization of N -Allenylindoles and N -Allenylpyrroles: An Access to Iododihydropyrido[1,2- a ]indoles and Dihydroindolizines

The formation of iodinated dihydropyrido[1,2- a ]indoles and dihydroindolizines was achieved by an iodocarbocyclization reaction of N -allenylindoles and N -allenylpyrroles. This transformation proceeded under very mild conditions using N -iodosuccinimide as the electrophilic iodine source to deliver the products via a 6- endo cyclization process. Careful choice of the solvent and concentration were mandatory to obtain the cyclization in good yields.

Efficient synthesis of 1-(2-propynyl)pyrrole

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