119325-92-7

Basic information

• Product Name: (CH₃)2CCCC(C₆H₅){Co(CH₃C(NOH)C(NO)CH₃)2C₅H₅N}
• CAS NO: 119325-92-7
• Molecular Weight: 523.538
• Mol File: 119325-92-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (CH₃)2CCCC(C₆H₅){Co(CH₃C(NOH)C(NO)CH₃)2C₅H₅N}(CAS DataBase Reference)
• NIST Chemistry Reference: (CH₃)2CCCC(C₆H₅){Co(CH₃C(NOH)C(NO)CH₃)2C₅H₅N}(119325-92-7)
• EPA Substance Registry System: (CH₃)2CCCC(C₆H₅){Co(CH₃C(NOH)C(NO)CH₃)2C₅H₅N}(119325-92-7)

Safety Data

• Hazardous Substances Data: 119325-92-7(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 16940-66-2 sodium tetrahydroborate 
• 95-45-4 butane-2,3-dione dioxime 
• 100108-99-4 Trifluoro-methanesulfonic acid 2-methyl-1-phenylethynyl-propenyl ester 

Relevant articles and documents

Formation of (σ-butatrienyl)- and (σ-enynyl)cobaloxime complexes via reaction of (dimethylglyoximato)(pyridine)cobalt anion, [Co(dmgH)2py]-, with alkynylvinyl triflates. Stereochemistry and mechanism of formation

Alkynylvinyl triflates readily react with [Co(dmgH)2py]- (4) to give either (σ-enynyl)- or (σ-butatrienyl)cobaloxime complexes depending upon the substitution pattern of the starting inflate. Reaction of either isomeric vinyl triflate 2E or 2Z gives only a single product enynyl complex 13E. In contrast reaction of isomeric vinyl triflates 3E and 3Z with 4 is stereospecific, presumably with retention of olefin geometry, giving only the respective (σ-butatrienyl)cobaloxime complexes. A double nucleophilic vinylic substitution is invoked to rationalize these results.