1416431-76-9

Basic information

• Product Name: C₂₄H₂₇NO₂
• Synonyms: C₂₄H₂₇NO₂
• CAS NO: 1416431-76-9
• Molecular Weight: 361.484
• Mol File: 1416431-76-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₄H₂₇NO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₄H₂₇NO₂(1416431-76-9)
• EPA Substance Registry System: C₂₄H₂₇NO₂(1416431-76-9)

Safety Data

• Hazardous Substances Data: 1416431-76-9(Hazardous Substances Data)

Upstream product

• 536-90-3 m-Anisidine 
• 766-85-8 3-methoxy-1-iodobenzene 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 92248-06-1 3-methoxy-N-(3-methoxyphenyl)benzenamine 

Downstream Products

• 1416431-78-1 1,8-dimethoxy-10-p-tert-butylphenylacridone 
• 1416431-82-7 C₅₁H₅₀N₂O₄ 
• 1416431-93-0 C₅₀H₄₇N₂O₄⁽¹⁺⁾*Cl₆Sb^(1-) 

Relevant articles and documents

Impact of diradical character on two-photon absorption: Bis(acridine) dimers synthesized from an allenic precursor

The two-photon absorption (TPA) of a bis(acridine) dimer (8) having singlet diradical character in its ground state was found to be enhanced by more than 2 orders of magnitude as compared to its closed-shell counterpart (12), which has the same structural backbone and atom composition. The dimer, a tetracation species consisting of two connected acridinium cation moieties with high coplanarity, was obtained during our attempts to synthesize triplet carbenes by double oxidation of an allenic precursor (3b). High conjugation over the two aromatic rings connected by dimerization was revealed by X-ray analysis, and a small HOMO-LUMO gap was found in the visible-near-infrared one-photon absorption spectrum in solution and in the crystalline state, exhibiting that the ground state of 8 has singlet diradical nature. Ab initio molecular orbital calculations of the ground state also suggested that 8 has an intermediate diradical character (y) of 0.685. Interconversion between diradical tetracation dimer 8 and closed-shell dication dimer 12 was achieved by oxidation/reduction in good yields and was accompanied by formation of monoradical trication dimer 13 as an intermediate. TPA measurements at near-infrared wavelengths revealed that diradical dimer 8 has large TPA cross sections (3600 GM at 1200 nm), while closed-shell 12 has TPA cross sections of a straightforward comparison between the TPA activity of molecules with the same structural backbone and atom composition but with different degree of the diradical character, supporting the theoretical prediction that enhanced TPA intensity can be observed in the intermediate y region (0 y 1).