1309151-10-7

Basic information

• Product Name: (2,4,6-triisopropylphenyl)ethynyl piperidine-1-carbodithioate
• Synonyms: (2,4,6-triisopropylphenyl)ethynyl piperidine-1-carbodithioate
• CAS NO: 1309151-10-7
• Molecular Weight: 387.654
• Mol File: 1309151-10-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2,4,6-triisopropylphenyl)ethynyl piperidine-1-carbodithioate(CAS DataBase Reference)
• NIST Chemistry Reference: (2,4,6-triisopropylphenyl)ethynyl piperidine-1-carbodithioate(1309151-10-7)
• EPA Substance Registry System: (2,4,6-triisopropylphenyl)ethynyl piperidine-1-carbodithioate(1309151-10-7)

Safety Data

• Hazardous Substances Data: 1309151-10-7(Hazardous Substances Data)

Upstream product

• 98-77-1 piperidinium piperidyldithiocarbamate 
• 1309151-28-7 2-oxo-2-(2,4,6-triisopropylphenyl)ethyl piperidine-1-carbodithioate 
• 110-89-4 piperidine 

Downstream Products

• 1351992-62-5 2-(piperidin-1-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolanyl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiole 
• 1351992-71-6 2,4-bis-(S-phenylthio)-2-(piperidin-1-yl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiole 
• 1351992-70-5 2-(1-methylhydrazin-1-yl)-2-(piperidin-1-yl)-4-(2,4,6-triisopropylphenyl)-1,3-dithiole 
• 1351992-65-8 2-(piperidin-1-yl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiolium-4-carboxylate 
• 1351992-68-1 2-diethylphosphino-2-(piperidin-1-yl)-4-(2,4,6-triisopropylphenyl)-1,3-dithiole 
• 1351992-61-4 2-(piperidin-1-yl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiolium-4-trifluoroborate 
• 1351992-60-3 4-bromo-2-(piperidin-1-yl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiolium bromide 
• 1351992-66-9 2-(piperidin-1-yl)-5-(2,4,6-triisopropylphenyl)-1,3-dithiolium-4-thiolate 
• 1351992-63-6 2-(2,6-dimethylphenylthio)-2-(piperidin-1-yl)-4-(2,4,6-triisopropylphenyl)-1,3-dithiole 
• 1351992-64-7 2-methoxy-2-(piperidin-1-yl)-4-(2,4,6-triisopropylphenyl)-1,3-dithiole 

Relevant articles and documents

A stable acyclic ligand equivalent of an unstable 1,3-dithiol-5-ylidene

Substitutes you can rely on: Mesoionic carbenes (MICs) are not always stable. However, the acyclic ethynylcarbamodithioate 2 formed (instead of the corresponding MIC) by deprotonation of dithiolium salt 1 underwent cyclization to its precursor under acidic conditions and reacted with a variety of transition-metal centers to yield robust MIC complexes 3; (see scheme; Tipp=2,4,6-triisopropylphenyl). Copyright