6405-28-3

Basic information

• Product Name: N-Benzyl-3,3'-iMinodipropionic Acid
• Synonyms: N-Benzyl-3,3'-iMinodipropionic Acid;N-Benzyl-3,3'-iminodipropionic Acid
• CAS NO: 6405-28-3
• Molecular Formula: C₁₃H₁₇NO₄
• Molecular Weight: 251.27838
• Mol File: 6405-28-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 157.0 to 161.0 °C
• Appearance: /
• Storage Temp.: -20°C Freezer
• Solubility: DMSO (Slightly, Sonicated), Water (Slightly, Sonicated)
• CAS DataBase Reference: N-Benzyl-3,3'-iMinodipropionic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyl-3,3'-iMinodipropionic Acid(6405-28-3)
• EPA Substance Registry System: N-Benzyl-3,3'-iMinodipropionic Acid(6405-28-3)

Safety Data

• Hazardous Substances Data: 6405-28-3(Hazardous Substances Data)

Usage

General Description

N-Benzyl-3,3'-iMinodipropionic Acid is a compound that belongs to the family of amino acids and is commonly used in the synthesis of peptides and proteins. It contains a benzyl group, which is a common organic moiety in many chemical compounds. N-Benzyl-3,3'-iMinodipropionic Acid has two amino groups and a carboxylic acid group, making it a building block for the synthesis of more complex molecules. It is used in various industrial and research applications, particularly in the production of pharmaceuticals and agrochemicals. This chemical has potential applications in the fields of medicine, agriculture, and materials science due to its unique structure and properties.

Upstream product

• 6938-07-4 N,N-bis(2-ethoxycarbonylethyl)benzylamine 
• 100-46-9 benzylamine 
• 79-10-7 acrylic acid 

Downstream Products

• 5192-03-0 5-amino-1H-indole 

Relevant articles and documents

New polynuclear compounds based on N-benzyliminodipropionic acid: solution studies, synthesis, and X-ray crystal structures

Three new polynuclear compounds based on a dicarboxylic acid ligand are reported. In particular, two Cu(II) coordination compounds, [Cu2(H2O)6(Hbzlidp)2](CF3SO3)2·2H2O (1) and [Cu(NO3)(Hbzlidp)]∞ (2) (bzlidp2??=?N-benzyliminodipropionate anion), and a Ni(II) dinuclear compound, [Ni2(H2O)4(bzlidp)2] (3), were synthesized and characterized by IR spectroscopy, elemental analysis and single crystal X-ray diffraction. Different structures were obtained depending on the reaction conditions. The structural analyses reveal that 1 was formed by dinuclear [Cu2(H2O)6(Hbzlidp)2]2+ units built by two copper(II) ions joined through two Hbzlidp? ligands, while 2 was formed by pairs of Cu(II) centers bridged by four syn,syn carboxylate groups to generate “paddle wheel” units. The dinuclear copper units are arranged in a rhombus type grid, in a 2-D layer structure. In both cases, the N was protonated and not coordinated to the metal center. Compound 3 was formed by [Ni2(H2O)4(bzlidp)2] neutral dinuclear units, with octahedral Ni(II) centers. Solution studies of the ligand–M(II) systems (M(II)?=?Mn, Co, Ni, Cu, Zn, Cd, and Pb) were also carried out.

Natural phosphate and potassium fluoride doped natural phosphate: Efficient catalysts for the construction of a carbon-nitrogen bond

The application of natural phosphates doped with potassium fluoride as heterogeneous catalysts for the Michael addition of aromatic and aliphatic amines to α,β-unsaturated carbonyl compounds is presented. The natural phosphate catalyst can be regenerated and reused without loss of activity, which makes it an attractive alternative to homogeneous basic reagents. Doping natural phosphate with potassium fluoride significantly enhances the rate and yield of the reaction.