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

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. This chemical has two amino groups and a carboxylic acid group, making it a building block for the synthesis of more complex molecules. Due to its unique structure and properties, N-Benzyl-3,3'-iMinodipropionic Acid has potential applications in various fields, including medicine, agriculture, and materials science.

Uses

Used in Pharmaceutical Industry:
N-Benzyl-3,3'-iMinodipropionic Acid is used as a building block for the synthesis of pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
N-Benzyl-3,3'-iMinodipropionic Acid is used as a component in the production of agrochemicals. Its properties make it suitable for the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Materials Science:
N-Benzyl-3,3'-iMinodipropionic Acid is used as a precursor in the synthesis of advanced materials. Its unique structure and properties can contribute to the development of new materials with specific characteristics for various applications.
Used in Research Applications:
N-Benzyl-3,3'-iMinodipropionic Acid is used as a research tool in various scientific studies. Its unique structure and properties make it a valuable compound for investigating new chemical reactions and exploring its potential uses in different fields.

Upstream product

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

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.