4936-89-4

Usage

Chemical structure

A propanediol molecule with a substituted phenyl ring and an amino group.

Building block

Commonly used in the synthesis of various polymeric materials and pharmaceuticals.

Antiseptic properties

Presence of the dibromo-2-hydroxyphenyl group makes it potentially useful for its antiseptic and antimicrobial properties.

Reactivity

The hydroxymethyl group adds to its reactivity and potential utility in chemical reactions.

Applications

Has a variety of potential applications in materials science, pharmaceuticals, and biomedical research.

Molecular weight

Approximately 342.99 g/mol

Appearance

It may appear as a colorless to pale yellow solid or liquid, depending on its purity and concentration.

Solubility

Soluble in polar solvents such as water, methanol, and ethanol.

Stability

Stable under normal temperature and pressure conditions, but sensitive to heat, light, and moisture, which may cause degradation over time.

Upstream product

• 90-59-5 3,5-Dibromosalicylaldehyde 
• 77-86-1 2-amino-2-hydroxymethyl-1,3-propanediol 

Relevant academic research and scientific papers

Syntheses and characterization of mononuclear Zn(II), Cd(II) and Hg(II) complexes of 2-[(3,5-dibromo-2-hydroxy-benzylidene)-amino]-2-hydroxymethyl-propane-1,3-diol: Photoluminescence properties and DFT study

A new Schiff-base ligand HL ((2-[(3,5-dibromo-2-hydroxy-benzylidene)-amino]-2-hydroxymethyl-propane-1,3-diol)) was obtained by the 1:1 condensation of 1,3-dibromo salicylaldehyde and (tris hydroxy methyl) amino methane. Then three new complexes, [Zn(L)su

Imine or Enamine? Insights and Predictive Guidelines from the Electronic Effect of Substituents in H-Bonded Salicylimines

Imine and enamine bonds decorate the skeleton of numerous reagents, catalysts, and organic materials. However, it is difficult to isolate at will a single tautomer, as dynamic equilibria occur easily, even in the solid state, and are sensitive to electronic and steric effect, including π-conjugation and H-bonding. Here, using as model Schiff bases generated from salicylaldehydes and TRIS in a set of linear free energy relationships (LFER), we disclose how the formation of either imines or enamines can be controlled and provide a comprehensive framework that captures the structural underpinning of this prediction. This work highlights the potentiality of tailor-made designs en route to compounds with desirable functionality.

Inner complex compounds of dioxomolybdenum(VI) with o-oxyazomethines, derivatives of substituted salicylaldehydes and tris(hydroxymethyl)aminomethane. crystal structures of two complexes [MoO(L)] · CH3OH; L = Z-substituted salicylalimines, Z =

Ten new dioxomolybdenum(VI) compounds with o-oxyazomethines, derivatives of substituted salicylaldehydes (I-X) and tris(hydroxymethyl)aminomethane, are synthesized. The structures of two of them, [MoO2(L)] · CH3OH; L = Z-substituted