67108-96-7

Basic information

• Product Name: C₃₈H₂₃BrN₄Ni
• Synonyms: C₃₈H₂₃BrN₄Ni
• CAS NO: 67108-96-7
• Molecular Weight: 674.221
• Mol File: 67108-96-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: C₃₈H₂₃BrN₄Ni(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₈H₂₃BrN₄Ni(67108-96-7)
• EPA Substance Registry System: C₃₈H₂₃BrN₄Ni(67108-96-7)

Safety Data

• Hazardous Substances Data: 67108-96-7(Hazardous Substances Data)

Upstream product

• 67066-09-5 5-bromo-10,20-dihexyl-15-phenylporphyrin (5) 
• 21211-65-4 di(pyrrol-2-yl)methane 
• 100-52-7 benzaldehyde 
• 67108-97-8 (5,10,15-triphenylporphyrinato)nickel(II) 
• 6018-89-9 nickel(II) acetate tetrahydrate 
• 591-51-5 phenyllithium 
• 22112-89-6 5,15-diphenylporphyrin 
• 67108-97-8 (5,10,15-triphenylporphyrinato)nickel(II) 

Downstream Products

• 67108-97-8 (5,10,15-triphenylporphyrinato)nickel(II) 
• 883148-67-2 E-5-(2-methoxycarbonylethenyl)-10,15,20-triphenylporphyrinatonickel(II) 
• 915719-46-9 [5-hydroxy-10,15,20-triphenylporphyrinato]nickel(II) 
• 175444-04-9 5-formyl-10,20-bis(3,5-di-tert-butylphenyl)Ni^IIporphyrin 
• 915719-45-8 di[(10,15,20-triphenylporphyrinato-5-yl)nickel(II)]amine 
• 915719-44-7 5-amino-10,15,20-triphenylporphyrinatonickel(II) 
• 1160725-09-6 C₄₁H₂₆N₄Ni 
• 1160725-11-0 C₄₁H₂₆N₄Ni 
• 1279603-65-4 9,10-bis[(10,15,20-triphenylporphyrin-5-ylato)nickel(II)]anthracene 
• 67108-97-8 (5,10,15-triphenylporphyrinato)nickel(II) 
• 869883-11-4 C₇₆H₄₆N₈Ni₂ 
• 1063613-09-1 [5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-10,15,20-triphenylporphyrinato]nickel(II) 
• 915719-47-0 5-carboxymethyl-10,15,20-triphenylporphyrinatonickel(II) 
• 1160725-11-0 [5,10,15-triphenyl-20-propadienylporphyrinato]nickel(II) 

Relevant articles and documents

Preparation of meso-silylporphyrins via nickel-catalyzed coupling of meso-brominated Ni(II) porphyrins with silylzinc reagents

– In this paper, we developed a technique for the nickel-catalyzed coupling of meso-brominated Ni(II) porphyrins with silylzinc reagents in order to prepare meso-silyl-substituted Ni(II) porphyrins. Porphyrin silylation occurs under mild conditions and ex

Synthesis and reactivity of allenylporphyrins

Several different methods have been utilized for the effective synthesis of a new class of porphyrins that contains the synthetically intriguing propadienyl (or allenyl) functional group. Of these approaches, successive Horner-Wadsworth-Emmons couplings p

Synthesis and ligand binding properties of triptycene-linked porphyrin arrays

Multiporphyrin arrays are a complex class of molecules with numerous potential applications in energy transfer, photomedicine, and light harvesting. We have developed a facile/versatile route to a class of triptycene-linked porphyrin arrays via both Suzuk