1341774-51-3

Basic information

• Product Name: 3-(2,6-diisopropylphenyl)-4,5,6,7,8,9-hexahydrocycloocta[d]thiazole-2(3H)-thione
• CAS NO: 1341774-51-3
• Molecular Weight: 359.6
• Mol File: 1341774-51-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(2,6-diisopropylphenyl)-4,5,6,7,8,9-hexahydrocycloocta[d]thiazole-2(3H)-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2,6-diisopropylphenyl)-4,5,6,7,8,9-hexahydrocycloocta[d]thiazole-2(3H)-thione(1341774-51-3)
• EPA Substance Registry System: 3-(2,6-diisopropylphenyl)-4,5,6,7,8,9-hexahydrocycloocta[d]thiazole-2(3H)-thione(1341774-51-3)

Safety Data

• Hazardous Substances Data: 1341774-51-3(Hazardous Substances Data)

Upstream product

• 39261-18-2 2-bromocyclooctan-1-one 
• 502-49-8 cycloactanone 

Downstream Products

• 1341774-69-3 3-(2,6-diisopropylphenyl)-4,5,6,7,8,9-hexahydrocycloocta[d]thiazol-3-ium perchlorate 

Relevant articles and documents

A family of thiazolium salt derived N-heterocyclic carbenes (NHCs) for organocatalysis: Synthesis, investigation and application in cross-benzoin condensation

A family of thiazolium salt derived N-heterocyclic carbenes (NHCs) bearing sterically demanding aryl substituents on the nitrogen and with varying backbone substitution patterns have been synthesized. Investigation of the catalytic activity of these NHCs in a number of benzoin-type coupling reactions revealed markedly different levels of reactivity and selectivity. To elucidate the underlying factors leading to differences in reactivity, a study of the electronic and steric properties of these NHC catalysts was conducted. By using the best catalyst in this study, the intermolecular cross-benzoin condensation reaction was explored in more detail.