1311297-12-7

Basic information

• Product Name: 1,3-bis(2,6-diisopropylphenyl)-1H-imidazole-2(3H)-thione
• Synonyms: 1,3-bis(2,6-diisopropylphenyl)-1H-imidazole-2(3H)-thione
• CAS NO: 1311297-12-7
• Molecular Weight: 420.662
• Mol File: 1311297-12-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1,3-bis(2,6-diisopropylphenyl)-1H-imidazole-2(3H)-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis(2,6-diisopropylphenyl)-1H-imidazole-2(3H)-thione(1311297-12-7)
• EPA Substance Registry System: 1,3-bis(2,6-diisopropylphenyl)-1H-imidazole-2(3H)-thione(1311297-12-7)

Safety Data

• Hazardous Substances Data: 1311297-12-7(Hazardous Substances Data)

Upstream product

• 244187-81-3 1,3-bis-(2,6-diisopropylphenyl)-imidazol-2-ylidene 
• 91-13-4 α,α'-dibromo-o-xylene 
• 10544-50-0 sulfur 
• 74663-75-5 1,2-bis(2,6-diisopropylphenylimino)ethane 
• 258278-25-0 1,3-bis[(2,6-diisopropyl)phenyl]imidazolinium chloride 
• 578743-87-0 chloro[1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]copper(I) 
• 250285-32-6 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride 
• 1207373-12-3 1,3-bis(2,6-diisopropylphenyl)imidazolium trifluoroacetate 
• 1311297-02-5 1,3-bis(2,6-diisopropylphenyl)imidazolium p-methylbenzenesulfonate 
• 1311297-01-4 1,3-bis(2,6-diisopropylphenyl)imidazolium nitrate 
• 1311296-99-7 1,3-bis(2,6-diisopropylphenyl)imidazolium perchlorate 
• 1311297-00-3 1,3-bis(2,6-diisopropylphenyl)imidazolium methanesulfonate 

Relevant articles and documents

Lewis-base stabilized diiodine adducts with N-heterocyclic chalcogenamides

Oxidation reactions of stable chalcogenamides with iodine are intriguing due to their broad application in various organic syntheses. In the present study we report on the utilization of N-heterocyclic carbene and cyclic-alkyl-amino carbenes L1-3/su

Saturated NHC Derived Dichalcogen Dications

Herein, the synthesis and characterization of dicationic dichalcogenide compounds [(SIPr)E]2(OTf)2 (3a-E) (E = S, Se, Te) based on a saturated N-heterocyclic carbene (NHC), SIPr [SIPr = C{N(Dipp)CH2}2, Dipp = 2,

A Mechanistically and Operationally Simple Route to Metal–N-Heterocyclic Carbene (NHC) Complexes

We have been puzzled by the involvement of weak organic and inorganic bases in the synthesis of metal–N-heterocyclic carbene (NHC) complexes. Such bases are insufficiently strong to permit the presumed required deprotonation of the azolium salt (the carbe