108357-17-1

Basic information

• Product Name: 1-(2-hydroxy-3-{4-[(4-nitrophenyl)carbonyl]phenoxy}propyl)-4-phenylpyridinium chloride
• CAS NO: 108357-17-1
• Molecular Formula: C₂₇H₂₃ClN₂O₅
• Molecular Weight: 490.9349
• Mol File: 108357-17-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2-hydroxy-3-{4-[(4-nitrophenyl)carbonyl]phenoxy}propyl)-4-phenylpyridinium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-hydroxy-3-{4-[(4-nitrophenyl)carbonyl]phenoxy}propyl)-4-phenylpyridinium chloride(108357-17-1)
• EPA Substance Registry System: 1-(2-hydroxy-3-{4-[(4-nitrophenyl)carbonyl]phenoxy}propyl)-4-phenylpyridinium chloride(108357-17-1)

Safety Data

• Hazardous Substances Data: 108357-17-1(Hazardous Substances Data)

Usage

Chemical structure

A complex compound derived from pyridinium with multiple functional groups, including a hydroxy group, a nitrophenyl carbonyl group, and a phenyl group.

Functional groups

Contains a hydroxy group (-OH), a nitrophenyl carbonyl group (-NO2-C6H4-CO-), and a phenyl group (-C6H5).

Presence of a chloride ion

The compound also contains a chloride ion (Cl-), which may contribute to its properties and potential applications.

Potential applications

Due to its unique structure and functional groups, the compound may have potential applications in various fields, such as pharmaceuticals or other industries.

Research interest

The compound's complex structure and multiple functional groups make it an interesting target for further research to explore its properties and potential uses.

Solubility

The presence of a hydroxy group and a chloride ion may affect the compound's solubility in different solvents, which could be relevant for its applications.

Reactivity

The compound's functional groups may participate in various chemical reactions, such as substitution, addition, or elimination reactions, depending on the reaction conditions and the presence of other reactants.

Stability

The presence of a nitro group and a carbonyl group in the compound may affect its stability under different conditions, such as temperature, pH, or exposure to light.

Optical properties

The compound's structure, including the phenyl and nitrophenyl groups, may result in specific optical properties, such as absorption or emission spectra, which could be useful for applications in sensors or imaging.

Biological activity

The compound's structure and functional groups may impart biological activity, making it a potential candidate for further investigation into its effects on biological systems or as a starting point for drug development.

Upstream product

• 939-23-1 p-phenylpyridine 

Relevant articles and documents

Phenyl-pyridinium salts and use thereof in inhibiting intestinal resorption

Polycyclic salts of the formula wherein A- is the anion of a strong organic or inorganic acid; XN+ is pyridinium, pyrimidinium, thiazolium or imidazolium substituted by R1, R2 and R3 ; n, q and r individually are the integer 1 or 0 and p is an integer from 1 to 15; Y is CH2, C(H,OH) or C(O): Z is O, S, CH2, C(O), NQ1, SO2, C(O)O, OC(O), C(O)N(Q1) or N(Q1)C(O); L is p-phenylene substituted by R4 ; and M is phenyl substituted by R5 and R6, T has one of the meanings given above, for Z or is C(CH3)2, C2 H4, C(Q2)=C(Q3), C C, CH2 C(O), C(O)CH2, CH2 O or OCH2, R1 is a group Ar, Ar-C1-4 -alkyl, ArO or ArC(O), Ar is phenyl substituted by R7, R8 and R9 ; R2 and R3 individually are H, C1-4 -alkyl, C1-4 -alkoxy or C6 H5, with the proviso that the N-atom in the 3-position of an imidazolium group XN+ is substituted by Ar, Ar-C1-4 -alkyl or C1-4 -alkyl, R4, R5, R6, R7, R8 and R9 individually are H, halogen, CF3, NO2, CN, C1-4 - -(alkyl, alkoxy, alkylthio or alkylsulphonyl), SO2 N(R,Q), C(O)N(Q4,Q5), C(O)Q4, C(O)OQ4 or OC(O)Q4, R, Q, Q1, Q2 and Q3 individually are H or C1-4 -alkyl, and Q4 and Q5 individually are C1-4 -alkyl inhibit the intestinal resorption of cholesterol and of bile salts in the enterohepatic circulation. These salts containing a quaternary N-atom can be manufactured starting from corresponding amines.