951174-49-5

Basic information

• Product Name: (3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID
• Synonyms: (3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID;(S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOICACID
• CAS NO: 951174-49-5
• Molecular Formula: C11H15NO4
• Molecular Weight: 225.2411
• Mol File: 951174-49-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID(951174-49-5)
• EPA Substance Registry System: (3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID(951174-49-5)

Safety Data

• Hazardous Substances Data: 951174-49-5(Hazardous Substances Data)

Usage

General Description

(3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID is a chemical compound that belongs to the class of amino acids. It is a derivative of proline, an essential amino acid that plays a crucial role in protein synthesis and overall cellular function. The presence of the amino group and the dimethoxyphenyl group makes this compound important in the field of medicinal chemistry, as it can potentially be used as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its specific chemical structure and properties make it a valuable tool for researchers in drug discovery and development.

Upstream product

• 6972-61-8 2,4-dimethoxycinnamic acid 
• 951174-16-6 tert-butyl (E)-3-(2,4-dimethoxyphenyl)propenoate 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 951174-32-6 tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(2,4-dimethoxyphenyl)propanoate 
• 306769-07-3 tert-butyl (S)-3-amino-3-(2,4-dimethoxyphenyl)propanoate 
• 951174-24-6 tert-butyl (3R,αS)-3-(N-benzyl-N-α-methylbenzylamino)-3-(2,4-dimethoxyphenyl)propanoate 
• 951174-41-7 tert-butyl (R)-3-amino-3-(2,4-dimethoxyphenyl)propanoate 
• 141-82-2 malonic acid 
• 72071-66-0 3-(2,4-Dimethoxy-phenyl)-3-hydroxyamino-propionic acid 

Downstream Products

• 138621-71-3 3-(2,4-Dimethoxy-phenyl)-3-(2,2,2-trifluoro-acetylamino)-propionic acid 

Relevant articles and documents

Parallel synthesis of homochiral β-amino acids

The parallel asymmetric synthesis of an array of 30 β-amino acids of high enantiomeric purity using the conjugate addition of homochiral lithium N-benzyl-N-(α-methylbenzyl)amide as the key step is accomplished. The experimental simplicity and highly practical nature of the protocol is demonstrated by the efficient parallel conversion of 15 α,β-unsaturated esters to both enantiomeric series of the corresponding β-amino acids in high overall yields and selectivities with minimal purification involved in each step of the reaction protocol.

One-Pot Cyclization of Alkoxy-3-Aminoindan-1-ones.

3-Amino-3-alkoxyphenylpropionic acids, prepared from alkoxybenzaldehydes, are cyclized in one step into 3-aminoindan-1-ones using trifluoroacetic acid and trifluoroacetic anhydride. Key Words: One-pot cyclization; Aminoindanones; Electrodonating substitue