936571-93-6

Basic information

• Product Name: 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde
• Synonyms: 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde
• CAS NO: 936571-93-6
• Molecular Weight: 199.252
• Mol File: 936571-93-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde(936571-93-6)
• EPA Substance Registry System: 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde(936571-93-6)

Safety Data

• Hazardous Substances Data: 936571-93-6(Hazardous Substances Data)

Upstream product

• 78075-83-9 1-benzyl-2-methyl-1H-pyrrole 
• 68-12-2 N,N-dimethyl-formamide 
• 1003-29-8 2-pyrrole aldehyde 
• 100-39-0 benzyl bromide 
• 64435-30-9 N⁵,N⁵,N¹⁰,N¹⁰-tetramethyl-5,10-dihydrodipyrrolo[1,2-a:1',2'-d]pyrazine-5,10-diamine 
• 74-88-4 methyl iodide 

Relevant articles and documents

Serendipitous base catalysed condensation-heteroannulation of iminoesters: a regioselective route to the synthesis of 4,6-disubstituted 5-azaindoles

A serendipitous discovery of a novel one-pot synthesis of 4,6-disubstituted 5-azaindoles is reported herein. In the presence of Hunig's base, various N-substituted pyrrole-2-carboxaldehydes have been efficiently transformed into their corresponding 4,6-disubstituted 5-azaindoles through an imine mediated cascade condensation-heteroannulation. The synthetic value of the methodology is established by preparing a novel chemical analogue of a cannabinoid receptor type 2 (CB2) agonist.

Multivalent indole compounds and use thereof as phospholipase-A2 inhibitors

Indole and indole-related compounds, compositions and methods are disclosed. The compounds of the invention are useful as phospholipase inhibitors. The compounds and compositions of the invention are useful for treatment of phospholipase-related conditions, such as insulin-related, weight-related and/or cholesterol-related conditions in an animal subject.