5066-50-2

Basic information

• Product Name: 4-[7-(benzyloxy)-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-methoxyphenol
• CAS NO: 5066-50-2
• Molecular Formula: C₂₄H₂₅NO₄
• Molecular Weight: 391.4596
• Mol File: 5066-50-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 560.7°C at 760 mmHg
• Flash Point: 292.9°C
• Density: 1.194g/cm³
• Vapor Pressure: 3.53E-13mmHg at 25°C
• Refractive Index: 1.603
• CAS DataBase Reference: 4-[7-(benzyloxy)-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-methoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[7-(benzyloxy)-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-methoxyphenol(5066-50-2)
• EPA Substance Registry System: 4-[7-(benzyloxy)-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]-2-methoxyphenol(5066-50-2)

Safety Data

• Hazardous Substances Data: 5066-50-2(Hazardous Substances Data)

Upstream product

• 2280-44-6 D-Glucose 
• 4245-37-8 vinyl methacrylate 
• 492-61-5 β-D-glucose 
• 760-93-0 methacryloyl anhydride 
• 920-46-7 Methacryloyl chloride 
• 2715-36-8 6-O-methacryloyl-1,2:3,4-di-O-isopropylidene-D-galactopyranose 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 7322-31-8 β-D-mannose 
• 10257-28-0 D-Galactose 

Relevant articles and documents

Gambogic acid-galactose-HPMA (N-(2-hydroxypropyl)methacrylamide) high-molecular copolymer, and preparation method and application thereof

The invention discloses a gambogic acid-galactose-HPMA (N-(2-hydroxypropyl)methacrylamide) high-molecular copolymer. The structural formula is shown as (I) in the specification. In the formula, x=5-10 mol%, y=5-10 mol%, z=80-90 mol%, Mn=2.2*10, and Mw/Mn=1.45. A preparation method comprises the following steps: preparing a galactose derivative C by taking D-galactose as a preparation raw material; reacting gambogic acid oxalamide and methylacryloyl to prepare a gambogic acid derivative D; and finally, performing condensation on the galactose derivative C, the gambogic acid derivative D and HPMA to obtain the gambogic acid-galactose-HPMA high-molecular copolymer. After being used in a drug for treating a neoplastic disease, the copolymer has a targeted intelligent drug release functional and achieves a favorable inhibition effect for liver cancer, lung cancer and colon cancer.

Intracellular protein delivery by glucose-coated polymeric beads

Glucose-coated polymeric beads have been prepared and applied to delivery of a model protein (enhanced green fluorescent protein) into mouse embryonic stem cells as well as Hela cells.

Differential activities of a lipase and a protease toward straight- and branched-chain acyl donors in transesterification to carbohydrates in an organic medium

Keywords: Lipases; Proteases; Acylation; Selective