125366-78-1

Usage

Uses

Used in Pharmaceutical Industry:
4,4'-dihydroxy-[1,1'-biphenyl]-3,3'-dicarbaldehyde is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Dyes Industry:
In the dyes industry, 4,4'-dihydroxy-[1,1'-biphenyl]-3,3'-dicarbaldehyde is used as a precursor for the production of various dyestuffs. Its ability to form stable chromophores makes it suitable for creating dyes with specific color properties.
Used in Organic Synthesis:
4,4'-dihydroxy-[1,1'-biphenyl]-3,3'-dicarbaldehyde is used as a versatile reagent in organic synthesis for the preparation of different functionalized biphenyls and related compounds. Its aldehyde and hydroxyl groups facilitate various chemical reactions, enabling the synthesis of a wide range of organic molecules.
Used as a Fluorescent Tag in Analytical Chemistry:
4,4'-dihydroxy-[1,1'-biphenyl]-3,3'-dicarbaldehyde is used as a fluorescent tag in analytical chemistry. Its inherent fluorescence properties allow for the detection and quantification of specific molecules in complex samples, making it a valuable tool in research and diagnostics.
Used as a Ligand in Coordination Chemistry:
In coordination chemistry, 4,4'-dihydroxy-[1,1'-biphenyl]-3,3'-dicarbaldehyde is used as a ligand to form coordination complexes with metal ions. Its ability to chelate metals provides opportunities for the development of new catalysts, sensors, and materials with unique properties.

Upstream product

• 67-66-3 chloroform 
• 92-88-6 4,4'-Dihydroxybiphenyl 
• 1222784-88-4 4-hydroxy-4'-methoxy-1,1'-biphenyl-3,3'-dicarbaldehyde 
• 1761-61-1 5-bromosalicyclaldehyde 
• 620595-36-0 2-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde 
• 76-05-1 trifluoroacetic acid 
• 2132-80-1 4,4'-Dimethoxybiphenyl 
• 50-00-0 formaldehyd 
• 100-97-0 hexamethylenetetramine 
• 93012-31-8 4,4'-dimethoxy-[1,1'-biphenyl]-3,3'-dicarbaldehyde 
• 1761-62-2 5-iodosalicyclaldehyde 

Relevant academic research and scientific papers

Exo-functionalized shape-persistent [2+3] cage compounds: Influence of molecular rigidity on formation and permanent porosity

Exo-functionalized [2+3] cage compounds were synthesized by using two different bissalicylaldehydes as molecular precursors in the reaction with triptycene triamine to study the influence of the rigidity of the molecular structure of [2+3] cages on their

The double oxa-Michael-aldol condensation: Straightforward access to dimeric tetrahydroxanthenones

Symmetrical dimeric tetrahydroxanthenones can be obtained in a single step starting from dimeric salicylic aldehydes and cyclohexenones employing a double oxa-Michael-aldol condensation. Georg Thieme Verlag Stuttgart.

Syntheses of 2,2′-bibenzo[7]annulenes by double Au-catalyzed sequential activation of propargylic carboxylates

We previously reported a novel Au-catalyzed sequential activation of two different propargyl carboxylates to 6-methylene-6H-benzo[7]annulene-5,8-diyl dicarboxylates. This reaction has been extended to syntheses of highly functionalized 2,2′-bibenzo[7]annulenes with four biphenyls bearing two sets of different propargyl carboxylates.

Rapid synthesis of novel and known coumarin-3-carboxylic acids using stannous chloride dihydrate under solvent-free conditions

Various coumarin-3-carboxylic acid (=2-oxo-2H-1-benzopyran-3-carboxylic acid; CcaH) derivatives have been synthesized in good yields using catalytic amounts of SnCl2·2 H2O under solvent-free conditions. This inexpensive, nontoxic, and readily available catalytic system (10 mol-%) efficiently catalyzes the Knoevenagel condensation and intramolecular cyclization of various 2-hydroxybenzaldehydes or acetophenones with Meldrum's acid. High product yields, use of inexpensive and safe catalyst, and solvent-free conditions display both economic and environmental advantages. Copyright

COLORANT COMPOSITION, PHOTOSENSITIVE RESIN COMPOSITION, PHOTO RESIST, COLOR FILTER, AND DISPLAY DEVICE

The color material composition of claim 1, wherein the compound is represented by the following formula. A photosensitive material, a color filter and a display device are provided. (by machine translation)

COLORANT COMPOSITION, PHOTOSENSITIVE RESIN COMPOSITION, PHOTO RESIST, COLOR FILTER, AND DISPLAY DEVICE

The present invention relates to a color material composition comprising a polymer including a unit represented by chemical formula 1, to a photosensitive resin composition comprising the same, to a photosensitive material, to a color filter, and to a dis

The polymerizable liquid crystal compound, the polymerizable composition, polymer, a phase difference film and its manufacturing method, a laminate for transfer, optical member and method of manufacturing same, and display device

A polymerizable liquid crystal compound which is represented by general formula (1). (In general formula (1), the symbols are as defined in the description.)

Synthesis and characterization of linear and macrocyclic ligands with multiple hemisalen pockets

Procedures for the convenient preparation of new ligands possessing multiple metal binding sites are presented. Among those, a Schiff base macrocycle exhibiting three outward hemisalen pockets was synthesized using a one-pot reduction/condensation reactio

Synthesis of tri-and disalicylaldehydes and their chiral schiff base compounds

A suitable procedure for convenient preparation of 1,3,5-tris(4-hydroxy-5- formylphenyl)benzene (6) was exploited via 5-bromosalicylaldehyde as starting reactant. Among the obtained products, compound 6, 4-methoxy-3- formylphenylboronic acid (9), 1,3,5-tris(4-methoxy-5-formylphenyl)benzene (10), and 4-methoxy-4'-hydroxyl-3,3'-diformyl-1,1'-diphenyl (11) had not been reported previously. Two new chiral Schiff base ligands, L1 and L2, were obtained from the tri-or disalicylaldehydes.

Synthesis of spiropyrans and merocyanine dyes based on 1-benzothieno[3,2-b] pyrrole

A convenient method was developed for the synthesis of photochromic spiropyrans and merocyanine dyes of the 1-benzothieno[3,2-b]pyrroline series based on the conventional condensation of the analog of Fischer's salt, viz., 1,2,3,3-tetramethyl-3H-[1]benzot