86629-66-5

Basic information

• Product Name: 1,3-Dioxan-2-one, 5-(phenylmethoxy)-
• Synonyms: 1,3-Dioxan-2-one,5-(phenylmethoxy);5-(benzyloxymethyl)-1,3-dioxan-2-one;5-benzyloxy-1,3-dioxan-2-one
• CAS NO: 86629-66-5
• Molecular Formula: C11H12O4
• Molecular Weight: 208.214
• Mol File: 86629-66-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxan-2-one, 5-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxan-2-one, 5-(phenylmethoxy)-(86629-66-5)
• EPA Substance Registry System: 1,3-Dioxan-2-one, 5-(phenylmethoxy)-(86629-66-5)

Safety Data

• Hazardous Substances Data: 86629-66-5(Hazardous Substances Data)

Usage

Type of compound

Cyclic carbonate derivative

Applications

a. Synthesis of various pharmaceuticals
b. Intermediate for the production of other chemicals

Biological activity

Exhibits some biological activity, potentially useful in the development of new drugs

Other potential uses

a. Insecticide
b. Component in various polymers and materials

Upstream product

• 14690-00-7 2-O-benzylglycerol 
• 541-41-3 chloroformic acid ethyl ester 
• 100-39-0 benzyl bromide 
• 68728-34-7 5-benzyloxy-2-phenyl-1,3-dioxane 

Relevant articles and documents

Dual-Targeted Cascade-Responsive Prodrug Micelle System for Tumor Therapy in Vivo

This study reports a cascade-responsive disassemble micellar drug delivery system with dual-targeting potential (cell and mitochondria targeting), which optimizes the distribution of antitumor drugs on systemic, local, and subcellular levels to enhance antitumor efficacy. A new cationic porphyrin derivative 5-(3-hydroxy-p-(4-trimethylammonium)butoxyphenyl)-10,15,20-triphenylporphyrin chlorine (MTPP) is synthesized as a mitochondria-targeting photosensitizer. After accumulating at a tumor site, the micellar nanosystem is endocytosed by tumor cells facilitated by the folate receptor-mediated pathway. Then, the hydrophobic PDEA block would be protonated in intracellular acidic endo-/lysosomes and promote the escape of prodrug micelles from endo-/lysosome to cytoplasm, resulting in the first-stage destabilization of micelles. Subsequently, the CPT is released in response to high concentration of GSH in cytoplasm, which would greatly increase the hydrophilicity of the BOH block and initiate the complete disassembly of the polymer micelles owing to the damage of the hydrophilic-hydrophobic balance. Additionally, the released MTPP is selectively accumulated in mitochondria and activates mitochondria apoptotic pathway upon light irradiation as a result of ROS generation. Both in vitro and in vivo studies indicate that the polymeric micelle not only effectively improves the targeted delivery efficiency but also dramatically enhances the combinational antitumor efficacy while reducing the side effects associated with the laser irradiation and mitochondria-targeted tumor therapy.

Polycarbonate and poly(carbonate-ester)s synthesized from biocompatible building blocks of glycerol and lactic acid

The synthesis and characterization of a polycarbonate of glycerol and poly(carbonate-ester)s of glycerol and L-lactic acid are reported. These new polymers possess a hydrolyzable backbone, tunable hydrophobic/hydrophilic properties, and functionalizable p