50802-66-9

Basic information

• Product Name: N-[2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide
• CAS NO: 50802-66-9
• Molecular Formula: C₁₆H₁₇NO₃
• Molecular Weight: 271.3111
• Mol File: 50802-66-9.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 529.9°C at 760 mmHg
• Flash Point: 274.3°C
• Density: 1.183g/cm³
• Vapor Pressure: 4.64E-12mmHg at 25°C
• Refractive Index: 1.588
• CAS DataBase Reference: N-[2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide(50802-66-9)
• EPA Substance Registry System: N-[2-hydroxy-2-(4-methoxyphenyl)ethyl]benzamide(50802-66-9)

Safety Data

• Hazardous Substances Data: 50802-66-9(Hazardous Substances Data)

Upstream product

• 56766-24-6 2-hydroxy-2-(4-methoxyphenyl)ethylammonium chloride 
• 98-88-4 benzoyl chloride 
• 6595-28-4 2-azido-1-(4-methoxyphenyl)ethan-1-one 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 637-69-4 4-Methoxystyrene 
• 123-11-5 4-methoxy-benzaldehyde 
• 144924-01-6 β-azido-α-(4-methoxyphenyl)ethanol 
• 66985-48-6 2-(4-methoxyphenyl)-2-(trimethylsilyloxy)acetonitrile 
• 55275-61-1 2-amino-1-(4-methoxyphenyl)ethanol 
• 65-85-0 benzoic acid 
• 15298-28-9 N-(2-hydroxy-2-(4-methoxyphenyl)ethyl)benzamide 
• 3672-47-7 3-oxo-3-(4'-methoxyphenyl)propanenitrile 
• 1393477-73-0 2-benzamido-1-(4-methoxyphenyl)ethyl hexanoate 
• 62921-42-0 5-(4-methoxyphenyl)-2-phenyl-1,3-oxazole 

Downstream Products

• 15298-31-4 1-acetoxy-2-benzoylamino-1-(4-methoxy-phenyl)-ethane 

Relevant articles and documents

Antibacterial compounds from zanthoxylum rhetsa

A new amide, zanthorhetsamide (1), along with nine known compounds (2-10) was isolated from the roots and stem barks of Zanthoxylum rhetsa. The structure was characterized by spectroscopic methods. In addition, the antibacterial activity of the isolates was evaluated. Dihydrochelerythrine (4) exhibited strong activity against methicillin-resistant Staphylococcus aureus SK1 and moderate activity against Escherichia coli TISTR 780 with MIC values of 8 and 16 μg/mL, respectively.

C3 The symmetry contains a chiral ligand H3L of an amide bond. Preparation method and application

The invention discloses C. 3 Chiral ligand H with symmetric amide bond3 L Relates to the technical field of material chemistry and chiral chemistry. The invention further provides the chiral ligand H. 3 L Preparation method and application thereof. The present invention has the advantage that the chiral ligand H of the present invention is a chiral ligand. 3 The L has a higher C. 3 The symmetric and flexible amide group enables coordination of the lanthanide metal ions with high coordination number and high oxygen affinity to be assembled into a novel structure-structure lanthanide metal chiral porous coordination cage. Moreover, the abundant chiral amide groups and amino acid residues on the ligand framework can be directly introduced into the synthesized lanthanide metal chiral porous coordination cage, thereby being beneficial to generating multiple chiral recognition sites and unique chiral microenvironments which mimic the biological enzyme binding pocket and further realize the purpose of high enantioselectivity separation of a series of chiral small molecule compounds.

Nitration-Peroxidation of Alkenes: A Selective Approach to β-Peroxyl Nitroalkanes

Nitration-peroxidation of alkenes for the synthesis of β-peroxyl nitroalkanes has been developed by using tert-butyl nitrite and tert-butyl hydroperoxide. The method presents a new and selective difunctionalization of alkenes to introduce a nitro group and a peroxyl group across the double bonds of alkenes under mild conditions. A radical reaction pathway is proposed by experimental and theoretical studies.