810670-02-1

Basic information

• Product Name: Methyl (R)-3-acetamido-3-(4-methoxyphenyl)propanoate
• Synonyms: (R)-methyl-3-acetamido-3-(4-methoxyphenyl)propanoate;METHYL (R)-3-ACETAMIDO-3-(4-METHOXYPHENYL)PROPANOATE
• CAS NO: 810670-02-1
• Molecular Formula: C13H17NO4
• Molecular Weight: 251.28
• Mol File: 810670-02-1.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 440.3oC at 760 mmHg
• Flash Point: 220.1oC
• Appearance: /
• Density: 1.129g/cm3
• Vapor Pressure: 5.97E-08mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: Methyl (R)-3-acetamido-3-(4-methoxyphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl (R)-3-acetamido-3-(4-methoxyphenyl)propanoate(810670-02-1)
• EPA Substance Registry System: Methyl (R)-3-acetamido-3-(4-methoxyphenyl)propanoate(810670-02-1)

Safety Data

• Hazardous Substances Data: 810670-02-1(Hazardous Substances Data)

Usage

General Description

Methyl (R)-3-acetamido-3-(4-methoxyphenyl)propanoate is a chemical compound with the molecular formula C14H19NO4. It is a methyl ester derivative of (R)-3-acetamido-3-(4-methoxyphenyl)propanoic acid. Methyl (R)-3-acetamido-3-(4-methoxyphenyl)propanoate is commonly used in pharmaceutical research and drug development due to its potential therapeutic properties. Its precise applications can vary, but it may be utilized in the synthesis of new medications or as a reference standard in analytical chemistry. The compound's structure and properties make it an important building block in organic synthesis and medicinal chemistry.

InChI:InChI=1/C13H17NO4/c1-9(15)14-12(8-13(16)18-3)10-4-6-11(17-2)7-5-10/h4-7,12H,8H2,1-3H3,(H,14,15)/t12-/m1/s1

Upstream product

• 108-24-7 acetic anhydride 
• 1333-74-0 hydrogen 
• 434957-24-1 (Z)-methyl 3-acetamido-3-(4-methoxyphenyl)-2-propenoate 
• 552838-52-5 methyl 3-acetamido-3-(4-methoxyphenyl)-2-propenoate 
• 22027-50-5 methyl 3-(4-methoxybenzoyl)acetate 
• 654061-84-4 methyl 3-amino-3-(4-methoxyphenyl)acrylate 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Relevant articles and documents

Nickel-catalyzed enantioselective umpolung hydrogenation for stereoselective synthesis of β-amido esters

Nickel complexes ligated by strongly donating diphosphines catalyze enantioselective hydrogenation for the preparation of acyclic and cyclic β-amido esters. A combination of acetic acid and indium powder provides protons and electrons to form nickel hydrido complexes under umpolung hydrogenation conditions.

Nickel-catalyzed asymmetric transfer hydrogenation of olefins for the synthesis of α- And β-amino acids

The field of asymmetric (transfer) hydrogenation of prochiral olefins has been dominated by noble metal catalysts based on rhodium, ruthenium, and iridium. Herein we report that a simple nickel catalyst is highly active in the transfer hydrogenation using

Highly efficient iridium-catalyzed asymmetric hydrogenation of unprotected β-enamine esters

A highly efficient and enantioselective hydrogenation of unprotected β-enamine esters catalyzed by Ir-(S,S)-f-Binaphane complex has been developed. This methodology provides straightforward access to free β-amino acids in high yields with excellent enantioselectivities up to 97% ee and high reactivities (TON > 5000).