194731-58-3

Basic information

• Product Name: Benzoic acid, 3,5-bis(benzoylamino)-
• CAS NO: 194731-58-3
• Molecular Formula: C21H16N2O4
• Molecular Weight: 360.369
• Mol File: 194731-58-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3,5-bis(benzoylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,5-bis(benzoylamino)-(194731-58-3)
• EPA Substance Registry System: Benzoic acid, 3,5-bis(benzoylamino)-(194731-58-3)

Safety Data

• Hazardous Substances Data: 194731-58-3(Hazardous Substances Data)

Upstream product

• 535-87-5 3.5-diaminobenzoic acid 
• 98-88-4 benzoyl chloride 

Downstream Products

• 266306-82-5 C₄₉H₃₆N₆O₈ 
• 328122-87-8 C₅₀H₃₈N₆O₈ 
• 1452406-51-7 C₄₉H₃₈N₆O₇ 
• 1452406-53-9 C₅₈H₅₃N₇O₈S₂ 
• 1452406-42-6 3,5-bis(benzoylamino)benzyl alcohol 
• 1452406-44-8 C₃₀H₃₃N₃O₄S₂ 
• 1254751-55-7 methyl 3,5-bis(benzoylamino)benzoate 

Relevant articles and documents

Well-defined thermoresponsive dendritic polyamide/poly(N-vinylcaprolactam) block copolymers

The first- and second-generation well-defined thermoresponsive amphiphilic linear-dendritic diblock copolymers based on hydrophilic linear poly(N-vinylcaprolactam) and hydrophobic dendritic aromatic polyamide have been synthesized via reversible addition fragmentation chain transfer polymerization of N-vinylcaprolactam by employing dendritic chain-transfer agents possessing a single dithiocarbamate moiety at the focal point. These linear-dendritic copolymers exhibit reversible temperature-dependent phase transition behaviors in aqueous solution as characterized by turbidity measurements using UV-vis spectroscopy. Their lower critical solution temperatures depend on the generation of the dendritic aromatic polyamides and the concentrations of the copolymer solutions. These amphiphilic copolymers are able to form nanospherical micelles in the aqueous solution as revealed by fluorescent spectroscopy, dynamic light scattering, and transmission electron microscope (TEM). The core-shell structure of micelles has been proved by 1H NMR analyses of the micelles in D2O. The micelles loaded with indomethacin as a model drug showed high-drug loading capacity and thermoresponsive drug release behavior.