109912-29-0

Basic information

• Product Name: N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE
• Synonyms: N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE;N-[2-[[(4-Methoxyphenyl)Methyl]-2-pyridinylaMino]ethyl]forMaMide
• CAS NO: 109912-29-0
• Molecular Formula: C₁₆H₁₉N₃O₂
• Molecular Weight: 285.34
• Product Categories: Aromatics;Intermediates;Amines;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 109912-29-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 527.9±45.0 °C(Predicted)
• Appearance: /
• Density: 1.167±0.06 g/cm3(Predicted)
• Solubility: Chloroform, Dichloromethane, Methanol
• PKA: 15.65±0.23(Predicted)
• CAS DataBase Reference: N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE(109912-29-0)
• EPA Substance Registry System: N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE(109912-29-0)

Safety Data

• Hazardous Substances Data: 109912-29-0(Hazardous Substances Data)

Usage

Description

N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE is a complex organic compound characterized by its light yellow oil appearance. It is an iodobolpyramine derivative, which is a class of compounds known for their potential applications in various fields due to their unique chemical properties.

Uses

Used in Pharmaceutical Industry:
N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE is used as a ligand for detecting histamine H1 receptors. This application is significant because histamine H1 receptors play a crucial role in various physiological processes and are often targeted in the treatment of conditions such as allergies, asthma, and other inflammatory diseases. The compound's ability to act as a ligand allows researchers to study the interaction between histamine H1 receptors and potential therapeutic agents, leading to the development of more effective medications.
Used in Chemical Research:
As an iodobolpyramine derivative, N'-FORMYL-N-(4-METHOXYBENZYL)-N-2-PYRIDINYL-1,2-ETHANEDIAMINE may also be used in chemical research to explore its potential applications in various fields. Its unique chemical structure and properties make it an interesting candidate for further investigation, which could lead to the discovery of new uses and applications in areas such as materials science, drug development, and environmental science.

Upstream product

• 74764-17-3 2-[(pyridin-2-yl)amino]ethylamine 
• 109-04-6 2-bromo-pyridine 

Downstream Products

• 109912-50-7 diiodobolpyramine 
• 109912-49-4 iodobolpyramine 
• 109912-48-3 bolpyramine 
• 109912-53-0 N'-(5-N-acetamidopentyl)-N-(4-methoxybenzyl)-N'-methyl-N-2-pyridinyl-1,2-ethanediamine 
• 110231-06-6 N¹-{2-[(4-Methoxy-benzyl)-pyridin-2-yl-amino]-ethyl}-N¹-methyl-heptane-1,7-diamine 
• 110231-08-8 N¹-{2-[(4-Methoxy-benzyl)-pyridin-2-yl-amino]-ethyl}-N¹-methyl-hexane-1,6-diamine 
• 109912-34-7 N'-(4-cyanobutyl)-N-(4-methoxybenzyl)-N'-methyl-N-2-pyridinyl-1,2-ethanediamine 
• 101395-32-8 N'-(5-aminopentyl)-N-(4-methoxybenzyl)-N'-methyl-N-2-pyridinyl-1,2-ethanediamine 
• 109912-41-6 N¹-{2-[(4-Methoxy-benzyl)-pyridin-2-yl-amino]-ethyl}-N¹-methyl-butane-1,4-diamine; compound with (Z)-but-2-enedioic acid 
• 109912-39-2 N¹-{2-[(4-Methoxy-benzyl)-pyridin-2-yl-amino]-ethyl}-N¹-methyl-propane-1,3-diamine; compound with (Z)-but-2-enedioic acid 
• 109912-37-0 N'-(2-aminoethyl)-N-(4-methoxybenzyl)-N'-methyl-N-2-pyridinyl-1,2-ethanediamine dimaleate 
• 109912-32-5 2-[4-({2-[(4-Methoxy-benzyl)-pyridin-2-yl-amino]-ethyl}-methyl-amino)-butyl]-isoindole-1,3-dione 
• 109912-31-4 2-[3-({2-[(4-Methoxy-benzyl)-pyridin-2-yl-amino]-ethyl}-methyl-amino)-propyl]-isoindole-1,3-dione 
• 109912-30-3 N-(4-methoxybenzyl)-N'-methyl-N'-(2-(N-phthalimido)ethyl)-N-2-pyridinyl-1,2-ethanediamine 

Relevant articles and documents

Iodobolpyramine and other iodinated derivatives as ligands for detecting histamine H1 receptors

The synthesis is described of potential I-labelled H1-receptor ligands.Receptor affinity is assessed in vitro from inhibition of histamine-stimulated contraction of guinea pig ileum and/or through binding to guinea pig cerebellar membranes.Dire