6876-71-7

Basic information

• Product Name: Pentanethioamide, N-(4-methylphenyl)-
• Synonyms: Thio-n-valeriansaeure-p-toluidid;Thiovaleriansaeure-p-toluidid;N-p-Tolyl-thiovaleramid
• CAS NO: 6876-71-7
• Molecular Formula: C12H17NS
• Molecular Weight: 207.34
• Mol File: 6876-71-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Pentanethioamide, N-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pentanethioamide, N-(4-methylphenyl)-(6876-71-7)
• EPA Substance Registry System: Pentanethioamide, N-(4-methylphenyl)-(6876-71-7)

Safety Data

• Hazardous Substances Data: 6876-71-7(Hazardous Substances Data)

Upstream product

• 693-03-8 n-butyl magnesium bromide 
• 622-59-3 1-isothiocyanato-4-methylbenzene 
• 109-72-8 n-butyllithium 
• 333-27-7 methyl trifluoromethanesulfonate 
• 1985-12-2 4-Bromophenyl isothiocyanate 

Downstream Products

• 5417-68-5 4-methyl-N-pentylbenzenamine 
• 7783-06-4 hydrogen sulfide 

Relevant articles and documents

Integrated Synthesis Using Isothiocyanate-Substituted Aryllithiums by Flow Chemistry

The isothiocyanate (NCS) group is an attractive functional group in the field of organic and pharmaceutical chemistry. It can be transformed into other heteroatomic functional groups. It usually acts as the inductive group of biological activity and has also been traditionally used as the fluorescent-labeling reagent. However, it is not compatible with strong bases. When the NCS group is at para position in halobenzenes, it generally undergoes nucleophilic additions upon reaction with strong bases. To the best of our knowledge, there is currently no general methodology for the formation and reactions of NCS-functionalized aryllithiums for meta and para substituents. Herein, we report the continuous-flow generation of NCS-substituted aryllithiums from the corresponding haloarenes via a selective halogen-lithium exchange reaction and its reaction with various electrophiles to yield NCS-containing products. We also achieved an integrated synthesis through sequential reactions of the NCS-containing compounds with additional nucleophiles using the continuous-flow reactors.