682803-14-1

Basic information

• Product Name: 2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID
• Synonyms: 3-AMINO-2-(4-METHOXYBENZYL)PROPANOIC ACID;2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID;RARECHEM AK HD CC33
• CAS NO: 682803-14-1
• Molecular Formula: C11H15NO3
• Molecular Weight: 209.24
• Product Categories: CHIRAL CHEMICALS
• Mol File: 682803-14-1.mol

Chemical Properties

• Boiling Point: 368.9°C at 760 mmHg
• Flash Point: 176.9°C
• Appearance: /
• Density: 1.175g/cm³
• Vapor Pressure: 4.3E-06mmHg at 25°C
• Refractive Index: 1.551
• CAS DataBase Reference: 2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID(682803-14-1)
• EPA Substance Registry System: 2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID(682803-14-1)

Safety Data

• Hazardous Substances Data: 682803-14-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research and Development:
2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID is used as a potential drug candidate for its ability to modulate certain biological processes, making it a valuable asset in the discovery and development of new medications.
Used in Anti-inflammatory Applications:
In the medical field, 2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID is used as an agent with potential anti-inflammatory properties, which can be beneficial in the treatment of various inflammation-related conditions.
Used in Analgesic Applications:
2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID is also used as an analgesic agent, indicating its potential effectiveness in managing pain and providing relief for individuals suffering from pain-related conditions.

InChI:InChI=1/C11H15NO3/c1-15-10-4-2-8(3-5-10)6-9(7-12)11(13)14/h2-5,9H,6-7,12H2,1H3,(H,13,14)

Relevant articles and documents

Catalytic Asymmetric Synthesis of Unprotected β2-Amino Acids

We report here a scalable, catalytic one-pot approach to enantiopure and unmodified β2-amino acids. A newly developed confined imidodiphosphorimidate (IDPi) catalyzes a broadly applicable reaction of diverse bis-silyl ketene acetals with a silylated aminomethyl ether, followed by hydrolytic workup, to give free β2-amino acids in high yields, purity, and enantioselectivity. Importantly, both aromatic and aliphatic β2-amino acids can be obtained using this method. Mechanistic studies are consistent with the aminomethylation to proceed via silylium-based asymmetric counteranion-directed catalysis (Si-ACDC) and a transition state to explain the enantioselectivity is suggested on the basis of density functional theory calculation.