152171-09-0

Basic information

• Product Name: 3-(1-hydroxyethyl)-1-tosylpyrrole
• Synonyms: 3-(1-hydroxyethyl)-1-tosylpyrrole
• CAS NO: 152171-09-0
• Molecular Weight: 265.333
• Mol File: 152171-09-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(1-hydroxyethyl)-1-tosylpyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-hydroxyethyl)-1-tosylpyrrole(152171-09-0)
• EPA Substance Registry System: 3-(1-hydroxyethyl)-1-tosylpyrrole(152171-09-0)

Safety Data

• Hazardous Substances Data: 152171-09-0(Hazardous Substances Data)

Upstream product

• 70-55-3 toluene-4-sulfonamide 
• 75-16-1 methylmagnesium bromide 
• 117954-70-8 3-formyl-1-<(4-methylphenyl)sulfonyl>pyrrole 
• 7126-39-8 pyrrole-3-carboxaldehyde 
• 98-59-9 p-toluenesulfonyl chloride 
• 106058-85-9 1-(1-tosyl-1H-pyrrol-3-yl)ethan-1-one 

Downstream Products

• 106058-85-9 1-(1-tosyl-1H-pyrrol-3-yl)ethan-1-one 
• 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 
• 199291-14-0 2-[1-(Toluene-4-sulfonyl)-1H-pyrrol-3-yl]-propionic acid 
• 152171-13-6 N-p-toluenesulfonyl-3-vinylpyrrole 

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

Gold(I)-catalyzed dearomative rautenstrauch rearrangement: Enantioselective access to cyclopenta[ b ]indoles

A highly enantioselective dearomative Rautenstrauch rearrangement catalyzed by cationic (S)-DTBM-Segphosgold(I) is reported. This reaction provides a straightforward method to prepare enantioenriched cyclopenta[b]indoles. These studies show vast differenc