152171-13-6

Basic information

• Product Name: N-p-toluenesulfonyl-3-vinylpyrrole
• Synonyms: N-p-toluenesulfonyl-3-vinylpyrrole
• CAS NO: 152171-13-6
• Molecular Weight: 247.318
• Mol File: 152171-13-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-p-toluenesulfonyl-3-vinylpyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: N-p-toluenesulfonyl-3-vinylpyrrole(152171-13-6)
• EPA Substance Registry System: N-p-toluenesulfonyl-3-vinylpyrrole(152171-13-6)

Safety Data

• Hazardous Substances Data: 152171-13-6(Hazardous Substances Data)

Upstream product

• 152171-09-0 3-(1-hydroxyethyl)-1-tosylpyrrole 
• 106058-85-9 1-(1-tosyl-1H-pyrrol-3-yl)ethan-1-one 
• 1138162-75-0 C₂₀H₂₈BNO₄S 
• 555-16-8 4-nitrobenzaldehdye 
• 70-55-3 toluene-4-sulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 63814-03-9 1,2,3,3a,4,5,12b,12c-octahydro-7H-1,3-benzodioxolo[5,6-c]pyrrolo[3,2,1-ij]quinoline 
• 1204777-41-2 1-p-toluenesulfonyl-7aα-(1-p-toluenesulfonyl-1H-pyrrol-3-yl)-4,5,6,7β-tetrahydro-1H-indole 
• 199291-14-0 2-[1-(Toluene-4-sulfonyl)-1H-pyrrol-3-yl]-propionic acid 
• 199291-08-2 2-[1-(Toluene-4-sulfonyl)-1H-pyrrol-3-yl]-propionaldehyde 

Relevant articles and documents

Asymmetric Organocatalytic Synthesis of Bisindoles – Scope and Derivatizations

Starting from 3-vinylindoles and glyoxolate imines, we created a library of diverse 4,6-bis(1H-indole-3-yl)piperidine 2-carboxylates by using 10 mol-% of a chiral phosphoric acid. Utilising electron-withdrawing groups on the starting material during the r

SN2′ boron-mediated Mitsunobu reactions - A new one-pot three-component synthesis of substituted enamides and enol benzoates

The conversion of (3-hydroxy-1-propen-1-yl)boronates to substituted enamides and enol benzoates is readily achieved in a one-pot procedure consisting of a regiocontrolled Mitsunobu reaction with convenient nucleophiles, followed by allylboration of aldehydes. Wiley-VCH Verlag GmbH & Co. KGaA, 2009.

Rhodium-catalyzed hydroformylation of 2-vinyl- and 3-vinyl-1-tosylpyrroles as a convenient synthetic route to the corresponding 2-(1-tosylpyrrolyl)propanals and derivatives

2-(1-Tosylpyrrolyl)propanals 2a-b were conveniently prepared (70% yield) via rhodium-catalyzed hydroformylation of the corresponding 2-vinyl- and 3-vinyl-1-tosylpyrroles 1a-b and successfully transformed into some new derivatives (50-90% yield).