618428-22-1

Basic information

• Product Name: 4,6-bis(1-methylhydrazinyl)-2-phenyl-1-pyrimidine
• Synonyms: 4,6-bis(1-methylhydrazinyl)-2-phenyl-1-pyrimidine
• CAS NO: 618428-22-1
• Molecular Weight: 244.299
• Mol File: 618428-22-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,6-bis(1-methylhydrazinyl)-2-phenyl-1-pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-bis(1-methylhydrazinyl)-2-phenyl-1-pyrimidine(618428-22-1)
• EPA Substance Registry System: 4,6-bis(1-methylhydrazinyl)-2-phenyl-1-pyrimidine(618428-22-1)

Safety Data

• Hazardous Substances Data: 618428-22-1(Hazardous Substances Data)

Upstream product

• 3740-92-9 fenclorim 
• 60-34-4 methylhydrazine 
• 618428-27-6 4,6-bis(1-methylhydrazino)-2-(3,4,5-trimethoxyphenyl)pyrimidine 
• 618428-41-4 4,6-bis{[N-methyl-N'-(pyridin-2-yl)methylidene]hydrazino}-2-phenylpyrimidine 
• 1670-14-0 benzamidine monohydrochloride 
• 13566-71-7 2-Phenyl-4,6-dihydroxy-pyrimidine 

Downstream Products

• 1361123-17-2 C₂₀H₂₀N₁₀ 
• 1230067-77-2 C₃₄H₄₀N₁₂ 
• 1230067-80-7 C₅₁H₆₀N₁₈ 
• 1230067-83-0 C₆₈H₈₀N₂₄ 
• 1230067-86-3 C₈₅H₁₀₀N₃₀ 
• 1230067-89-6 C₁₀₂H₁₂₀N₃₆ 
• 618428-70-9 2-phenylpyrimidine-4,6-dicarboxaldehyde bis{methyl{6-[1-methyl-2-(pyridin-2-ylmethylene)hydrazino]2-phenylpyrimidin-4-yl}hydrazone} 
• 618428-41-4 4,6-bis{[N-methyl-N'-(pyridin-2-yl)methylidene]hydrazino}-2-phenylpyrimidine 
• 618428-59-4 pyridine-2-carboxaldehyde methyl[6-(1-methylhydrazino)-2-phenylpyrimidin-4-yl]hydrazone 

Relevant articles and documents

Electronic absorption and emission properties of bishydrazone [2?×?2] metallosupramolecular grid-type architectures

Several ditopic ligands containing two tridentate bishydrazone coordination subunits and their Zn(II) and Cd(II) [2 × 2] grid-type complexes were prepared and their photoluminescent properties studied. A special attention was devoted to the influence of the orientation of the hydrazone group N–N[dbnd]in the core of the ligands and their complexes. Its reversal from [pyridine[dbnd]N–N–pyrimidine] (L1) to [pyridine–N–N[dbnd]pyrimidine] (L2) has a strong impact on the observed absorption and emission behaviour of particular ligands (L1 and L2) as well as of their [2 × 2] grid assemblies. The further lateral functionalization of the ligands led to different emission quantum yields of the resulting grids, while their emission and absorption spectra varied very little. The simplest derivative L1 turned out to have the best performance with, for its Zn(II) complex, relatively high quantum yield 60%.

Generation of dynamic constitutional diversity and driven evolution in helical molecular strands under Lewis acid catalyzed component exchange

A stir in the library: The efficient Sc(OTf)3-catalyzed transimination of helical oligo-hydrazone strands has been utilized to yield a highly diverse constitutional dynamic library through assembly, dissociation, and exchange of components. Thi