22657-66-5

Basic information

• Product Name: Benzenamine, 4,4'-cyclohexylidenebis[2,6-dimethyl-
• Synonyms: HMS1473L21
• CAS NO: 22657-66-5
• Molecular Formula: C22H30N2
• Molecular Weight: 322.494
• Mol File: 22657-66-5.mol
• Article Data: 7

Chemical Properties

• Melting Point: 185 °C
• Boiling Point: 477.1±45.0 °C(Predicted)
• Density: 1.064±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenamine, 4,4'-cyclohexylidenebis[2,6-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4,4'-cyclohexylidenebis[2,6-dimethyl-(22657-66-5)
• EPA Substance Registry System: Benzenamine, 4,4'-cyclohexylidenebis[2,6-dimethyl-(22657-66-5)

Safety Data

• Hazardous Substances Data: 22657-66-5(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 87-62-7 2,6-dimethylaniline 

Downstream Products

• 172788-71-5 N-<4-<1-(4-Amino-3,5-dimethylphenyl)cyclohexylidene>-2,6-dimethylphenyl>-3-<<4-<1-(4-amino-3,5-dimethylphenyl)cyclohexylidene>-2,6-dimethylphenyl>sulfonyl>benzamide 
• 252641-90-0 C₆H₁₀(C₆H₂(CH₃)2NHC(O)C₅H₃NC(O)NHC₅H₂(CH₃)2N)2 
• 299173-87-8 N-{4-[1-(4-amino-3,5-dimethyl-phenyl)-cyclohexyl]-2,6-dimethyl-phenyl}-N'-(2,6-diisopropyl-phenyl)-isophthalamide 
• 169179-52-6 N,N'-bis<4-<1-(4-amino-3,5-dimethylphenyl)cyclohexyl>-2,6-dimethylphenyl>-5-tert-butylisophthalamide 
• 141062-51-3 N,N'-bis{4-[1-(4-amino-3,5-dimethylphenyl)cyclohexylidene]-2,6-dimethylphenyl}isophthalic acid diamide 
• 1159594-16-7 N,N'-bis{4-[1-(4-amino-3,5-dimethylphenyl)cyclohexylidene]-2,6-dimethylphenyl}-2-fluoroisophthalamide 
• 169624-18-4 C₅₂H₆₁BrN₄O₂ 
• 643013-64-3 C₂₄H₂₈O₄ 
• 900780-77-0 C₇₄H₉₄N₆O₄Si₂ 

Relevant articles and documents

The effect of the linker size in C2-symmetrical chiral ligands on the self-assembly formation of luminescent triple-stranded di-metallic Eu(iii) helicates in solution

Chiral lanthanide-based supramolecular structures have gained significant importance in view of their application in imaging, sensing and other functional purposes. We have designed chiral C2-symmetrical ligands (L) based on the use of two 2,6-

NOVEL COMPOUND HAVING MULTIMER STRUCTURE OF XANTHENE DERIVATIVE, COLORING COMPOSITION, INK FOR INKJET RECORDING, METHOD OF INKJET RECORDING, COLOR FILTER, AND COLOR TONER

There is provided a compound represented by formula (1): in formula (1), L represents a divalent to tetravalent linking group; D represents a residue obtained by removing 1 to 5 hydrogen atoms from a compound represented by formula (2); m represents an integer of 1 to 10, however, each L may be the same with or different from every other L; n represents an integer of 2 to 10, however, each D may be the same with or different from every other D; and in formula (2), each of R4 to R24 independently represents a hydrogen atom or a substituent, provided that formula (2) has at least one or more ionic hydrophilic groups.

Energy transfer labels with mechanically linked fluorophores

Mechanically linked energy transfer labels comprising at least one donor fluorophore, at least one acceptor fluorophore, and at least one support member, wherein steric interactions between the donor fluorophore(s), the acceptor fluorophore(s), and/or the support member(s) induce non-covalent association between the fluorophores and the support member(s), thereby forming a three-dimensional macromolecular structure which mechanically links the donor fluorophore(s) and the acceptor fluorophore(s). Fluorescence resonance energy transfer (FRET) occurs from donor fluorophore to acceptor fluorophore through space. No direct connectivity with covalent bonds exists between the fluorophores. Instead, mechanical barriers hold the donor/acceptor fluorophores in place during the FRET process.