118159-39-0

Basic information

• Product Name: 2-nitro-5-(piperidin-1-yl)benzoic acid
• Synonyms: 2-nitro-5-(piperidin-1-yl)benzoic acid
• CAS NO: 118159-39-0
• Molecular Formula: C₁₂H₁₄N₂O₄
• Molecular Weight: 250.25056
• Mol File: 118159-39-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-nitro-5-(piperidin-1-yl)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-nitro-5-(piperidin-1-yl)benzoic acid(118159-39-0)
• EPA Substance Registry System: 2-nitro-5-(piperidin-1-yl)benzoic acid(118159-39-0)

Safety Data

• Hazardous Substances Data: 118159-39-0(Hazardous Substances Data)

Usage

General Description

2-nitro-5-(piperidin-1-yl)benzoic acid is a chemical compound with the molecular formula C13H14N2O4. It is a derivative of benzoic acid and contains a nitro group and a piperidine ring. 2-nitro-5-(piperidin-1-yl)benzoic acid has several potential applications, including use as a building block in the synthesis of pharmaceuticals and as a starting material for the preparation of various organic compounds. It is important to handle this compound with care, as it can be hazardous if not handled properly and should be stored and used in accordance with safety guidelines.

Upstream product

• 110-89-4 piperidine 
• 153437-56-0 4-chloro-6-piperidinoquinazoline 
• 2516-95-2 5-chloro-2-nitrobenzoic acid 
• 320-98-9 5-fluoro-2-nitrobenzoic acid 

Downstream Products

• 1339010-98-8 N-methyl-2-amino-5-(piperidin-1-yl)benzamide 
• 1339011-04-9 N-benzyl-2-amino-5-(piperidin-1-yl)benzamide 
• 1339011-10-7 2-(3-hydroxyphenyl)-3-methyl-6-(piperidin-1-yl)-1,2,3,4-tetrahydro-1H-quinazolin-4-one 
• 1339011-12-9 2-(4-hydroxyphenyl)-3-methyl-6-(piperidin-1-yl)-1,2,3,4-tetrahydro-1H-quinazolin-4-one 
• 1339011-23-2 2-phenyl-3-benzyl-6-(piperidin-1-yl)-1,2,3,4-tetrahydro-1H-quinazolin-4-one 
• 1339011-27-6 2-(3-hydroxyphenyl)-3-benzyl-6-(piperidin-1-yl)-1,2,3,4-tetrahydro-1H-quinazolin-4-one 
• 1339011-29-8 2-(4-hydroxyphenyl)-3-benzyl-6-(piperidin-1-yl)-1,2,3,4-tetrahydro-1H-quinazolin-4-one 
• 1339010-83-1 N-methyl-2-nitro-5-(piperidin-1-yl)benzamide 
• 1339010-89-7 N-benzyl-2-nitro-5-(piperidin-1-yl)benzamide 
• 1354652-83-7 2-nitro-5-(piperidin-1-yl)-N-(2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)benzamide 
• 1354653-05-6 methyl 3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzoate 
• 1354653-06-7 3-((2-((2-phenylpyrimidin-5-yl)carbamoyl)-4-(piperidin-1-yl)phenyl)carbamoyl)benzoic acid 
• 1354653-07-8 C₄₄H₅₄N₆O₈ 
• 1354652-69-9 C₄₀H₄₆N₆O₈ 

Relevant articles and documents

Dipole-mediated rectification of intramolecular photoinduced charge separation and charge recombination

Controlling charge transfer at a molecular scale is critical for efficient light harvesting, energy conversion, and nanoelectronics. Dipole-polarization electrets, the electrostatic analogue of magnets, provide a means for "steering" electron transduction via the local electric fields generated by their permanent electric dipoles. Here, we describe the first demonstration of the utility of anthranilamides, moieties with ordered dipoles, for controlling intramolecular charge transfer. Donor- Acceptor dyads, each containing a single anthranilamide moiety, distinctly rectify both the forward photoinduced electron transfer and the subsequent charge recombination. Changes in the observed charge- Transfer kinetics as a function of media polarity were consistent with the anticipated effects of the anthranilamide molecular dipoles on the rectification. The regioselectivity of electron transfer and the molecular dynamics of the dyads further modulated the observed kinetics, particularly for charge recombination. These findings reveal the underlying complexity of dipole-induced effects on electron transfer and demonstrate unexplored paradigms for molecular rectifiers.

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