124293-81-8

Basic information

• Product Name: 1H-Indole-3-carboxaldehyde, 2-methyl-1-(phenylsulfonyl)-
• CAS NO: 124293-81-8
• Molecular Formula: C16H13NO3S
• Molecular Weight: 299.35
• Mol File: 124293-81-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indole-3-carboxaldehyde, 2-methyl-1-(phenylsulfonyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-3-carboxaldehyde, 2-methyl-1-(phenylsulfonyl)-(124293-81-8)
• EPA Substance Registry System: 1H-Indole-3-carboxaldehyde, 2-methyl-1-(phenylsulfonyl)-(124293-81-8)

Safety Data

• Hazardous Substances Data: 124293-81-8(Hazardous Substances Data)

Upstream product

• 80360-20-9 1-(phenylsulfonyl)indole-3-carbaldehyde 
• 136878-55-2 3-((tert-butylimino)methyl)-1-(phenylsulfonyl)indole 
• 80360-21-0 1-(benzenesulfonyl)-2-methyl-1H-indole 
• 68-12-2 N,N-dimethyl-formamide 
• 136878-59-6 [1-(1-Benzenesulfonyl-2-methyl-1H-indol-3-yl)-meth-(E)-ylidene]-tert-butyl-amine 
• 95-20-5 2-methyl-1H-indole 
• 85678-41-7 N-benzenesulphonyl-2-methyl-3-thiophenoxyindole 

Downstream Products

• 1451192-90-7 C₂₅H₂₈N₂O₃S 
• 1451192-94-1 C₂₃H₂₄N₂O₂S 
• 1451192-89-4 C₂₇H₃₂N₂O₃S₂ 
• 1451192-93-0 C₂₉H₃₆N₂O₃S₂ 
• 1451192-88-3 C₂₈H₃₄N₂O₄S₂ 
• 1451192-92-9 C₂₈H₃₆N₂O₄S₂ 
• 1451192-86-1 C₂₉H₃₆N₂O₅S₂ 
• 1451192-91-8 C₂₆H₃₂N₂O₅S₂ 
• 3247-10-7 (-)-vincadifformine 
• 4429-63-4 tabersonine 
• 32975-46-5 (-)-1,2,14,15-tetradehydroaspidospermidine 
• 1448696-32-9 C₂₂H₂₃NO₄S 

Relevant articles and documents

First discovery of pimprinine derivatives and analogs as novel potential herbicidal, insecticidal and nematicidal agents

Pimprinine and streptochlorin are indole natural products produced by many species of organisms, and they are reported to possess a wide range of biological activities, such as anticancer, antiviral, antifungal activity and so on. In this study, three series of pimprinine derivatives or analogs were efficiently synthesized under the optimized methods. Biological assays conducted at Syngenta firstly indicated the pimprinine derivatives or analogs possessed potential herbicidal and insecticidal activity, and this is highlighted by compounds 21g, 21h, 21i, 21j, 21l, 22h, 22i and 23h, they possessed significant biological activity as well as broad spectrum. Meanwhile, compounds with benzothiophene-oxazole core (21h, 22h and 23h), showed effective nematicidal activity in primary screening. Compounds 21g and 21i were identified as the most promising lead structures for further study.

SYNTHETIC STUDIES ON INDOLE ALKALOIDS. IV. STUDIES OF N-PHENYLSULFONYL-2-METHYLINDOLES ON INTRAMOLECULAR CYCLIZATIONS

The synthesis of 1-(2-hydroxyethyl)-2--4-piperidone ethylene ketal (4) by two alternative ways and the study of its intramolecular cyclization using potassium tert-butoxide are reported.