79421-44-6

Basic information

• Product Name: 4-(4-HYDROXYPIPERIDIN-1-YL)BENZALDEHYDE
• Synonyms: 4-(4-HYDROXYPIPERIDIN-1-YL)BENZALDEHYDE;4-(4-Hydroxypiperidin-1-yl)benzaldehyde95%;4-(4-HYDROXYPIPERIDIN-1-YL)BENZALDEHYDE 95%;4-(4-Hydroxy-1-piperidinyl)benzaldehyde;Zinc02563693
• CAS NO: 79421-44-6
• Molecular Formula: C₁₂H₁₅NO₂
• Molecular Weight: 205.25
• Product Categories: API intermediates
• Mol File: 79421-44-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 401.516 °C at 760 mmHg
• Flash Point: 196.63 °C
• Appearance: /
• Density: 1.205 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.614
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-(4-HYDROXYPIPERIDIN-1-YL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-HYDROXYPIPERIDIN-1-YL)BENZALDEHYDE(79421-44-6)
• EPA Substance Registry System: 4-(4-HYDROXYPIPERIDIN-1-YL)BENZALDEHYDE(79421-44-6)

Safety Data

• Hazardous Substances Data: 79421-44-6(Hazardous Substances Data)

Usage

General Description

4-(4-Hydroxypiperidin-1-yl)benzaldehyde is a chemical compound belonging to the class of organic compounds known as phenylpiperidines, a subclass of piperidines. This substance is recognized as a moderately basic compound. Its chemical formula is C12H15NO2 and possesses an aromatic aldehyde group as a part of its molecular structure. While there might be limited information available on this chemical, it may be utilized in certain chemical reactions and processes due to the presence of functional groups that are reactive. For safety and handling, like most chemicals, appropriate measures should be taken.

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

• 79421-47-9 4-(4-Oxo-piperidin-1-yl)-benzaldehyde 
• 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 
• 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 
• 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 
• 1400538-26-2 1-(1H-benzo[d]imidazol-5-yl)-5-(4-(4-hydroxypiperidin-1-yl)phenyl)pyrrolidine-2,4-dione 
• 1246249-32-0 2-[4-(4-hydroxypiperidin-1-yl)phenyl]-5,7-dimethoxypyrido[2,3-d]pyrimidin-4(3H)-one 
• 1246249-97-7 5,7-dimethoxy-2-[4-(4-oxopiperidin-1-yl)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one 

Relevant articles and documents

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.

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

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.