1761-55-3

Usage

Appearance

Yellow-orange crystalline solid

Uses

Production of dyes and pigments
Manufacturing of rubber
Photographic developer

Toxicity

Considered toxic

Health risks

Potential carcinogenic and mutagenic effects

Regulatory status

Banned in some countries due to health risks

Safety precautions

Handle and use with caution, following safety regulations

Upstream product

• 1194-98-5 2,5-Dihydroxybenzaldehyde 
• 95-55-6 2-amino-phenol 

Relevant academic research and scientific papers

OH-substituted tridentate ONO Schiff base ligands and related molybdenum(VI) complexes for solvent-free (ep)oxidation catalysis with TBHP as oxidant

Molybdenum complexes with ONO tridentate Schiff base ligands based on salicylideneaminophenolato (SAP) backbone with OH substitution on the salicyl arene ring have been synthesized and characterized. The molecular structures of the full series of OH substituted molybdenum complexes were determined by X-ray crystallography as monomers stabilized by one solvent molecule, [MoO2L(D)]. All dimeric complexes [MoO2L]2 were tested for the epoxidation of cyclooctene and cyclohexene under organic solvent-free conditions using aqueous TBHP as oxidant. The position of the OH on the SAP-modified ligand influenced the catalytic activity of the respective complexes. DFT calculations for the catalytic cycle yield energy spans in agreement with the experimentally observed activity trend.

Benzylideneaniline derivatives

This invention describes a method of treating inflammation in warm blooded animals by topically administering an effective amount of benzylideneaniline or its derivatives.