86202-08-6

Upstream product

• 21563-29-1 4-bromo-1,8-naphthalene anhydride 
• 106-49-0 p-toluidine 
• 81-86-7 4-bromo-1,8-naphthalenedicarboxylic anhydride 

Downstream Products

• 1239450-85-1 N-(4-methylphenyl)-4-azido-1,8-naphthalimide 
• 90715-04-1 6-(2-hydroxy-ethoxy)-2-p-tolyl-benzo[de]isoquinoline-1,3-dione 

Relevant academic research and scientific papers

Substituted naphthalimide derivatives as well as preparation method and application thereof

The invention discloses substituted naphthalimide derivatives as well as a preparation method and application thereof. The substituted naphthalimide derivatives have a structure of a general formula D, wherein R1 is selected from n-butyl, phenyl, p-methyl

Naphthalimide derivative containing 4-(alkylbicyclohexyl) substitute, and preparation method and application thereof

The invention discloses a naphthalimide derivative containing a 4-(alkylbicyclohexyl) substitute, and a preparation method and application thereof. The naphthalimide derivative is of a structure represented by the general formula B, wherein R1 is one of a

Naphthalimide Aryl Sulfide Derivative Norrish Type i Photoinitiators with Excellent Stability to Sunlight under Near-UV LED

A series of Norrish type I photoinitiators (NASs), which are naphthalimide aryl sulfide derivatives, are prepared. The potential mechanism involved in the photolysis of NASs under UV LED at 405 nm is investigated by steady-state photolysis, nuclear magnet

Naphthalimide aromatic sulfide photoinitiator for UV-LED photocuring and preparation method and application thereof

The invention discloses a naphthalimide aromatic sulfide photoinitiator for UV-LED photocuring and relates to the field of light-sensing polymers. The photoinitiator herein is provided based on the problem that an existing photoinitiator has poor initiati

Excited-State Triplet Equilibria in a Series of Re(I)-Naphthalimide Bichromophores

We present the synthesis, structural characterization, electronic structure calculations, and the ultrafast and supra-nanosecond photophysical properties of a series of five bichromophores of the general structural formula [Re(5-R-phen)(CO)3(dm

Synthesis and photophysical properties of novel fluorescent materials containing 2,4,6-triphenylpyridine and 1,8-naphthalimide units using Suzuki reaction

A series of novel 2,4,6-triphenylpyridine derivatives containing 1,8-naphthalimide groups have been prepared in good yields using Suzuki couplings reactions. The relationship of the photoluminescence property of the compounds was systematically investigated via a thermogravimetric analyzer, UV-vis, fluorescence and electrochemical analyzer.

Water-solvent method for the synthesis of N-substituted and N-,4-disubstituted 1,8-naphthalimides under microwave irradiation

A preparation of a series of N-and N-,4-substituted 1,8-naphthalimides using water as solvent under microwave irradiation, which proceeded via efficient and green reaction of 1,8-naphthalic anhydride derivatives with different amines, is described.

FLUORESCENT BRIGHTENERS, METHODS OF PREPARATION THEREOF, FLUORESCENT BRIGHTENER COMPOSITIONS, AND METHODS OF PREPARATION AND USES THEREOF

A compound of Formula (I) wherein R1, R2, and R3 are independently at each occurrence hydrogen, a halogen, a cyano functionality, a C1-C20 aliphatic functionality, a C3-C10 cyclo

Synthesis of 4-aziridino [C60]fullerene-1,8-naphthalimide(C 60-NI dyads) and their photophysical properties

A series of 4-aziridino[C60]fullerene-1,8-naphthalimide (C 60-NI) dyads 4 ([6,6]-closed ring) were synthesized as the only addition product from the reaction of C60 with the corresponding azide compounds 3 under microwave

Fluorescent brighteners, methods of preparation thereof, fluorescent brightener compositions, and methods of preparation and uses thereof

A compound of Formula (I) wherein R1, R2, and R3 are independently at each occurrence hydrogen, a halogen, a cyano functionality, a C1-C20 aliphatic functionality, a C3-C10 cyclo