31352-40-6

Upstream product

• 128-08-5 N-Bromosuccinimide 
• 611-97-2 bis(p-methylphenyl)-methanone 
• 874-60-2 4-methyl-benzoyl chloride 
• 108-88-3 toluene 

Downstream Products

• 82313-76-6 4,4'-Bis(brommethyl)triphenylmethanol 
• 738606-68-3 3-{4-[4-(2-Ethoxycarbonyl-2-methylpropyl)-benzoyl]-phenyl}-2,2-dimethylpropionic acid ethyl ester 
• 1430325-27-1 4,4'-bis[(diethylphosphono)methyl]benzophenone 
• 114067-27-5 bis(bromomethylphenyl)methanol 
• 183166-22-5 3,5-Dimethyl-2-[4-[4-(4-phenylpiperazinylmethyl)benzoyl]benzylthio]-4-(3H)-quinazolinone 
• 1365571-82-9 C₃₁H₂₄N₆O 

Relevant academic research and scientific papers

Synthesis of a photoactive gemini surfactant and its use in AGET ATRP miniemulsion polymerisation and UV curing

A novel photoactive gemini surfactant was easily synthesised in high yields. The multi-functional molecule can be used as a gemini surfactant, a benzophenone type photoinitiator, and as an ATRP initiator. Poly(methyl methacrylate) (PMMA) and poly(methyl m

Persistent Radicals of Self-assembled Benzophenone bis-Urea Macrocycles: Characterization and Application as a Polarizing Agent for Solid-state DNP MAS Spectroscopy

UV-irradiation of a self-assembled benzophenone bis-urea macrocycle generates μm amounts of radicals that persist for weeks under ambient conditions. High-field EPR and variable-temperature X-band EPR studies suggest a resonance stabilized radical pair th

(4,4')BENZOPHENONO(2,6)NAPHTHALENOPHANE: SYNTHESIS, STRUCTURE, AND SPECTROSCOPIC STUDY

The synthesis of (4,4')benzophenono(2,6)naphthalenophane (1), the parent member of a series of stacked senzitizer-acceptor cyclophanes, is reported along with its x-ray structure and the absorption and emission spectra.

Synthesis of cardanol-based photo-active SET-LRP initiator and its application to preparation of UV-cured resin

A benzophenone-containing SET-LRP initiator based on renewable and abundant cardanol was synthesised in 71 % yield using the selective etherification reaction. Next, methyl methacrylate (MMA) as a monomer was polymerised under SET-LRP conditions using the

SYNTHESES AND REACTIONS OF SOME NEW DITHIAPARACYCLOPHANES AND PARACYCLOPHANES

The syntheses of new dithiaparacyclophanes and paracyclophanes are presented and their NMR spectroscopic properties are described.The possibility to synthesize new twin paracyclophanes by intramolecular coupling reactions of these cyclop

New Benzophenone-derived bisphosphonium salts as leishmanicidal leads targeting mitochondria through inhibition of respiratory complex II

A set. of benzophenone-derived bisphosphonium salts was synthesized and assayed for lethal activity on the human protozoan parasite Leishmania. A subset of them, mostly characterized by phosphonium substituents with an intermediate hydrophobicity, inhibit

Manipulating the cavity of a porous material changes the photoreactivity of included guests

Changing an ether to a ketone within the framework of a bis-urea macrocycle has little effect on the supramolecular assembly of this building block into porous crystals but introduces a triplet sensitizer into the framework that dramatically alters the ph

Synthesis, characterization, antibacterial activity and molecular docking studies on triazolophanes with benzophenone and S(-)-BINOL functionalization at the intra annular position

Triazolophanes with benzophenone and S(-)-BINOL functionalization at the intra annular position have been synthesized by the click reaction of 4,4′-bis(azidomethyl) benzophenone with the corresponding bispropargyloxy compounds. The newly synthesized triazolophanes were characterized by spectral and analytical methods. Triazolophane with S(-)-BINOL and benzophenone functionality at the intra annular position shows good target binding ability in molecular docking studies and also better antibacterial activity against all the four tested pathogens viz. Staphylococcus aureus, Bacillus subtilis, Salmonella typhimurium, and Escherichia coli bacteria.

ANTIBACTERIAL HYDROPHILIC COMPOUND AND USE THEREOF

The present disclosure provides an antibacterial hydrophilic compound. The antibacterial hydrophilic compound may react, induced by light through a hydrogen abstraction group in the structural formula thereof, with a C—H group and thus bind to a surface of a material having the C—H group (for example, chemical fibers such as polyester, chinlon, and the like; plastics, rubbers, and other similar materials), which can impart a durable antibacterial activity and hydrophilicity to the material. The antibacterial hydrophilic compound has a relatively strong binding force to the surface of the material without damaging the mechanical properties of the raw material. The present disclosure also provides a modified material that is modified by the antibacterial hydrophilic compound.

Antistatic compound, surface treatment method for material, and modified material

The present invention provides an antistatic compound. The antistatic compound is obtained by chemically reacting a compound with the structural formula represented by L1' or L2' with a compound Q', and the compound Q' is one or more of a polyhydroxy compound, a polycarboxy compound and a polysulfonate compound; L1' and L2' are shown in the description; and in the formulas L1' and L2', r is 1 or 2, Y is one of a single bond, the oxygen atom, the sulfur atom, the selenium atom, -C(O)-, -SO2-, -NH- and a C1-3 alkylene group, R1 to R10 and R to R are respectively independently selected from the hydrogen atom, a halogen atom, a monovalent polar group and a substituted or unsubstituted monovalent C1-18 hydrocarbon group, and at least one of the R1 to R10 or R to R reacts with the compound Q' to achieve chemical bonding. The antistatic compound can be combined with -CH- group-containing materials such as polyester and nylon to make the materials have antistatic properties and dyeability without reducing the mechanical properties of the materials.