79421-44-6

Usage

Uses

Used in Chemical Reactions and Processes:
4-(4-Hydroxypiperidin-1-yl)benzaldehyde is used as a reactive compound in various chemical reactions and processes due to the presence of its functional groups. Its aromatic aldehyde group allows for a range of chemical transformations, making it a versatile building block in organic synthesis.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(4-Hydroxypiperidin-1-yl)benzaldehyde may be used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity can contribute to the development of new drugs with potential therapeutic applications.
Used in Research and Development:
4-(4-Hydroxypiperidin-1-yl)benzaldehyde can be utilized in research and development settings to explore its chemical properties, reactivity, and potential applications in various fields. This may include studying its interactions with other compounds, evaluating its stability, and investigating its use in the synthesis of novel materials or molecules with specific functions.

InChI:InChI=1/C12H15NO2/c14-9-10-1-3-11(4-2-10)13-7-5-12(15)6-8-13/h1-4,9,12,15H,5-8H2

Upstream product

• 5382-16-1 4-HYDROXYPIPERIDINE 
• 459-57-4 4-fluorobenzaldehyde 

Downstream Products

• 1400538-26-2 1-(1H-benzo[d]imidazol-5-yl)-5-(4-(4-hydroxypiperidin-1-yl)phenyl)pyrrolidine-2,4-dione 
• 1246249-97-7 5,7-dimethoxy-2-[4-(4-oxopiperidin-1-yl)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one 
• 1246249-32-0 2-[4-(4-hydroxypiperidin-1-yl)phenyl]-5,7-dimethoxypyrido[2,3-d]pyrimidin-4(3H)-one 
• 942949-43-1 1-(4-{6-Bromo-7-[4-(1-phenyl-ethyl)-piperazin-1-yl]-3H-imidazo[4,5-b]pyridin-2-yl}-phenyl)-piperidin-4-ol 
• 942950-85-8 2-(4-(6-Chloro-2-(4-(4-hydroxypiperidin-1-yl)phenyl)-3H-imidazo[4,5-b]pyridin-7-yl)piperazin-1-yl)-N-(thiazol-2-yl)acetamide 
• 1095381-23-9 1-(4-(6-bromo-7-(4-((2-methylthiazol-4-yl)methyl)piperazin-1-yl)-3H-imidazo[4,5-b]pyridin-2-yl)phenyl)piperidin-4-ol 
• 79421-47-9 4-(4-Oxo-piperidin-1-yl)-benzaldehyde 

Relevant academic research and scientific papers

Synthesis of high molar extinction coefficient push-pull tricyanofuran-based disperse dyes: Biological activity and dyeing performance

Several push-pull tricyanofuran-based disperse dyes with high molar extinction coefficient were synthesized and fully characterized. The dyes were preparedviaKnoevenagel reaction in dry pyridine under ambient conditions employing acetic acid as catalyst. The condensation process was carried out between the reactive methyl-bearing tricyanofuran moiety and tertiary amine-based arylaldehyde. The molecular structures of the synthesized chromophores were proved by Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic resonance spectroscopy (1H and13C NMR) and elemental analysis (C, H, N). The UV-Vis absorbance spectra of the synthesized dyes demonstrated interesting extinction coefficient values, which were found to be influenced by the aromatic-vinyl bridge and the tertiary amine donor group bonded to this aromatic-vinyl bridge moiety. The prepared tricyanofuran-based disperse colorants were dyed on polyester fabrics to afford satisfactory results. The substituents attached to the tertiary amine moiety influenced the absorption maxima. The fastness properties of the dyed polyester samples were measured. The biological activities of the synthesized dyestuffs against fungus (Candida Albican) as well as Gram-positive (S. Aureus) and Gram-negative (E. Coli) pathogens were also evaluated.

ORGANIC NONLINEAR OPTICAL IONIC CRYSTAL BASED ON MULTI-FUNCTIONAL ELECTRON-DONATING BUILDING　BLOCKS

Provided is an organic ion crystal exhibiting nonlinear optical properties by inducing non-centrosymmetric molecular arrangement through introduction of multifunctional electron-donating building blocks which show electron-donating properties and hydrogen

Multi-functional supramolecular building blocks with hydroxy piperidino groups: New opportunities for developing nonlinear optical ionic crystals

We report on multi-functional supramolecular building blocks for obtaining a non-centrosymmetric crystal structure, which is the essential requirement for achieving a macroscopic second-order nonlinear optical activity. The supramolecular building blocks

NOVEL IMIDAZOPYRIDINE DERIVATIVES AS A TYROSINE KINASE INHIBITOR

Provided is a novel imidazopyridine derivative having irreversible tyrosine kinase inhibiting activities, and a pharmaceutical composition comprising the same which can be useful for prevention or treatment of inflammatory diseases, autoimmune diseases, p

SUBSTITUTED 1-AMINOPHTHALAZINE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC APPLICATION THEREOF

The invention concerns 1-amino-phthalazine derivatives of general formula (I): Wherein A, B, L, R, R1, R2, R3, R4, R5 and R7 are as defined herein. The invention also concerns the preparation of said compounds and their therapeutic use.

Amphiphilic nonlinear optical bis-chromophores and their mixtures with amphotropic copolymers: Preparation of monolayers and Langmuir - Blodgett multilayers

A new type of bis-chromophores containing two successive, covalently linked, nonlinear optical (NLO) dyes has been synthesized. For their preparation, α-cyanocinnamates or dinitrophenylhydrazones have been combined with an 4′-alkoxybiphenyl-4-carboxylate