Anthranilic acid

Application 2-(Hydroxymethyl)anthraquinone (a photoremovable protecting group) was used to chemically cage ( Z )-11-hexadecen-1-ol (sex pheromone of Chilo infuscatellus snellen ) .

9,10-Anthracenedicarboxylic acid (H 2 L) is an anthracene based dicarboxylic compound, which has a larger conjugating &#960-system that enables the development of fluorescent materials. It has interesting magnetic and luminescent properties.

The Diels-Alder reaction of 9-anthracenecarboxaldehyde with benzenediazonium-2-carboxylate was studied . Application 9-Anthracenecarboxaldehyde has been used in the synthesis of: new asymmetrical tridentate Schiff base ligands

The Diels-Alder reaction of 9-anthracenecarboxaldehyde with benzenediazonium-2-carboxylate was studied . Application 9-Anthracenecarboxaldehyde has been used in the synthesis of: new asymmetrical tridentate Schiff base ligands

The Diels-Alder reaction of 9-anthracenecarboxaldehyde with benzenediazonium-2-carboxylate was studied . Application 9-Anthracenecarboxaldehyde has been used in the synthesis of: new asymmetrical tridentate Schiff base ligands

Application Ajmalicine (&#948-Yohimbine, Py-Tetrahydroserpentine, Raubasine) is an alkaloid used to study its effects as an antagonist of adrenergic and nicotinic receptors. Biochem/physiol Actions Metabolite in the indole alkaloid biosynthesis

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Application Anthraflavic acid can be used as a starting material to synthesize tetrahydroxy tetrathiafulvalene (TTF) derivatives, which are used as redox-active building blocks in supramolecular and materials science. It is also utilized to prepare

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Application Used for non-selective, efficient fluorescent labeling of glycans. Slightly less sensitive than anthranilic acid (2-AA) for glycan labeling.

Application Fluorescently labels glycans containing a free reducing terminus. Used for non-selective, efficient fluorescent labeling of glycans.

Application Fluorescently labels glycans containing a free reducing terminus. Used for non-selective, efficient fluorescent labeling of glycans.