58107-25-8

Usage

Uses

Used in Pharmaceutical Synthesis:
1,3-Benzenedicarboxaldehyde, 5-fluoro-2-hydroxyis used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Dye Production:
1,3-Benzenedicarboxaldehyde, 5-fluoro-2-hydroxyis utilized as a precursor in the production of dyes, where its unique structure can influence the color and properties of the resulting dyes.
Used in Organic Compound Synthesis:
1,3-Benzenedicarboxaldehyde, 5-fluoro-2-hydroxyis used as a building block in the synthesis of a variety of organic compounds, taking advantage of its reactive functional groups and structural features to create diverse molecules with specific applications.
Used in Material Development:
1,3-Benzenedicarboxaldehyde, 5-fluoro-2-hydroxyis employed in the development of new materials, where its unique structure can contribute to the creation of materials with novel properties for various industrial applications.
Used in Biomolecule Development:
1,3-Benzenedicarboxaldehyde, 5-fluoro-2-hydroxyis used in the design and synthesis of biomolecules, potentially leading to advancements in areas such as biomedicine and biotechnology.

Upstream product

• 371-41-5 4-Fluorophenol 
• 100-97-0 hexamethylenetetramine 

Downstream Products

• 1585257-64-2 C₁₉H₂₀FN₄NiO₄⁽¹⁺⁾*ClO₄^(1-) 
• 100-02-7 4-nitro-phenol 

Relevant academic research and scientific papers

Development of a near-infrared ratiometric fluorescent probe for glutathione using an intramolecular charge transfer signaling mechanism and its bioimaging application in living cells

A novel near-infrared (NIR) ratiometric fluorescent probe HBT-GSH derived from conjugated benzothiazole was developed for the selective detection of glutathione (GSH) over cysteine (Cys) and homocysteine (Hcy). The probe was sophisticatedly designed based

Readily prepared inclusion forming chiral calixsalens

Calixsalens, chiral triangular hexaimines are readily synthesized by [3 + 3] cyclocondensation of trans-(R,R)-1,2-diaminocyclohexane with 2-hydroxyisophthalaldehyde derivatives. The usually rigid calixsalen ring is able to invert its conformation as a consequence of steric repulsion between bulky substituents at the C5 positions of the aromatic rings. The steric and electronic nature of the substituents does not affect only the conformation of the macrocycle. Small polar substituents enforce dimeric self-association to form an apohost where each of the monomers simultaneously serves as the host and the guest of its partner. Non-associating calixsalens form assemblies in which two symmetry-related molecules are arranged in a head-to-head fashion to form a capsule, or unimolecular cages that are able to entrap solvent molecules in their intrinsic voids.