70978-88-0

Basic information

• Product Name: 4-(2-METHOXYETHOXY)PIPERIDINE
• Synonyms: 4-(2-METHOXYETHOXY)PIPERIDINE;UKRORGSYN-BB BBV-066461;4-(2-methoxyethoxy)piperidine(SALTDATA: FREE)
• CAS NO: 70978-88-0
• Molecular Formula: C₈H₁₇NO₂
• Molecular Weight: 159.22608
• Mol File: 70978-88-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 220.1°C at 760 mmHg
• Flash Point: 85.3°C
• Appearance: /
• Density: 0.97g/cm³
• Vapor Pressure: 0.115mmHg at 25°C
• Refractive Index: 1.453
• CAS DataBase Reference: 4-(2-METHOXYETHOXY)PIPERIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-METHOXYETHOXY)PIPERIDINE(70978-88-0)
• EPA Substance Registry System: 4-(2-METHOXYETHOXY)PIPERIDINE(70978-88-0)

Safety Data

• Hazardous Substances Data: 70978-88-0(Hazardous Substances Data)

Usage

General Description

The chemical 4-(2-methoxyethoxy)piperidine is a compound with the molecular formula C9H19NO2. It is also known by the name "MEP." This chemical is a piperidine derivative that is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It is a colorless liquid with a mild, sweet odor and is soluble in water, making it suitable for use in aqueous formulations. MEP is also known to have mild irritant properties, but is generally considered to be a relatively low-risk chemical. Its main applications include its use as a solvent, intermediate, or reagent in organic synthesis.

InChI:InChI=1/C8H17NO2/c1-10-6-7-11-8-2-4-9-5-3-8/h8-9H,2-7H2,1H3

Upstream product

• 4045-22-1 N-acetyl-4-hydroxypiperidine 
• 6482-24-2 2-Bromoethyl methyl ether 
• 800401-96-1 tert-butyl 4-(2-methoxyethoxy)piperidine-1-carboxylate 
• 109384-19-2 t-butyl 4-hydroxy piperidine-1-carboxylate 
• 141047-46-3 N-formyl-4-hydroxypiperidine 
• 5382-16-1 4-HYDROXYPIPERIDINE 
• 141047-54-3 N-formyl-4-(1,4-dioxapentyl)piperidine 

Downstream Products

• 141062-22-8 (S)-2-{(S)-1-Benzyl-2-[4-(2-methoxy-ethoxy)-piperidin-1-yl]-2-oxo-ethylamino}-hexanoic acid ((1S,2R,3S)-1-cyclohexylmethyl-2,3-dihydroxy-5-methyl-hexyl)-amide 
• 1056877-75-8 C₁₅H₂₃N₃O₄ 

Relevant articles and documents

Preparation and application of aminourea-sensitive amine oxidase inhibitor

The invention provides preparation and application of an aminourea-sensitive amine oxidase inhibitor. Specifically, the invention discloses a compound as shown in a formula I which is described in thespecification or a stereoisomer or racemate or a pharmaceutically acceptable salt thereof. The invention also discloses the capability of the compound in inhibition of aminourea-sensitive amine oxidase.

Nonpeptide Renin Inhibitors Employing a Novel 3-Aza(or oxa)-2,4-dialkyl Glutaric Acid Moiety as a P2/P3 Amide Bond Replacement

A new series of renin inhibitors has been developed.The inhibitors feature a novel replacement for the P2/P3 dipeptide moiety normally associated with renin inhibitors.The dipeptide replacement was a (2S,4S)-3-aza(or oxa)-2,4-dialkylglutaric acid amide.Ex

Antihypertensive 4-amino-2-[4-(substituted-alkoxy)piperidino)]quinazolines

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