1195-51-3

Basic information

• Product Name: 4-[2-(aminooxy)ethyl]morpholine dihydrochloride
• CAS NO: 1195-51-3
• Molecular Formula: C₆H₁₄N₂O₂*2ClH
• Molecular Weight: 219.1094
• Mol File: 1195-51-3.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 331.1°C at 760 mmHg
• Flash Point: 154.1°C
• Vapor Pressure: 0.000114mmHg at 25°C
• CAS DataBase Reference: 4-[2-(aminooxy)ethyl]morpholine dihydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[2-(aminooxy)ethyl]morpholine dihydrochloride(1195-51-3)
• EPA Substance Registry System: 4-[2-(aminooxy)ethyl]morpholine dihydrochloride(1195-51-3)

Safety Data

• Hazardous Substances Data: 1195-51-3(Hazardous Substances Data)

Usage

General Description

4-[2-(aminooxy)ethyl]morpholine dihydrochloride is a chemical compound that is used in scientific research and pharmaceutical applications. It is a dihydrochloride salt of 4-[2-(aminooxy)ethyl]morpholine, which is a derivative of morpholine. 4-[2-(aminooxy)ethyl]morpholine dihydrochloride has a wide range of potential uses, including as a biochemical tool for studying protein function and as a potential therapeutic agent. It has been studied for its ability to act as a selective inhibitor of certain enzymes and its potential to modulate biological processes. In addition, this compound has been investigated for its potential to be used in the treatment of various diseases, making it a subject of interest for further research and development.

Upstream product

• 622-40-2 2-(morpholin-4-yl)ethanol 
• 606143-97-9 (2-Morpholin-4-yl-ethoxy)-carbamic acid tert-butyl ester 
• 3647-69-6 4-(2-chloroethyl)morpholine hydrochride 
• 3240-94-6 N-(2-chlorethyl)morpholine 
• 98883-94-4 benzophenone O-(2-morpholin-4-yl-ethyl)-oxime 
• 6261-84-3 propan-2-one O-2-morpholinoethyl oxime 

Downstream Products

• 6261-95-6 1-(2-morpholin-4-yl-ethoxy)-3-phenyl-thiourea 
• 61819-94-1 4-isopropyl-benzaldehyde O-(2-morpholin-4-yl-ethyl)-oxime 
• 6261-96-7 1-(4-ethoxy-phenyl)-3-(2-morpholin-4-yl-ethoxy)-thiourea 
• 33440-38-9 4-phenyl-but-3-en-2-one O-(2-morpholin-4-yl-ethyl)-oxime 
• 112772-28-8 2,6-Dimethyl-5-{1-[(E)-2-morpholin-4-yl-ethoxyimino]-ethyl}-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3-carboxylic acid methyl ester 
• 785725-31-7 (2,3-Dichloro-4-methoxy)-phenyl 2-thienyl O-(morpholinoethyl)-ketone oxime 
• 944341-54-2 JNJ-28871063 

Relevant articles and documents

HYDROXAMATE COMPOUNDS AS ANTAGONISTS OF THE ADENOSINE A2A RECEPTOR

The present invention relates to compounds of formula I shown below: (I) wherein R1, R2 and R3 are each as defined in the application. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of diseases or conditions in which adenosine A2a receptor activity is implicated, such as, for example, cancer.

MODULATORS OF HYPOXIA INDUCIBLE FACTOR-1 AND RELATED USES

The invention features compounds of formula (I): and pharmaceutically acceptable salts and prodrugs thereof, as well methods for modulating the effects of local and systemic hypoxic events using the compounds.

FUSED HETEROCYCLIC COMPOUND

A compound of the formula: wherein ring'' A is a 7-membered or 8-membered nitrogen- containing ring optionally further substituted, ring B is an optionally substituted aryl group or an optionally substituted heteroaryl group, X1 is a group represented by -NR3-Y1-, -0-, -S-, -SO-, -SO2- or -CHR3- wherein R3 is a hydrogen atom or'' an optionally substituted aliphatic hydrocarbon group, or R3 may be bonded to the carbon atom of ring B to form an optionally substituted ring structure, and Y1 is a bond or an optionally substituted C1-4 alkylene, R1 is a hydrogen atom, or an optionally substituted group bonded via a carbon atom or a sulfur atom, the formula = shows a single bond or a double bond, when ===R2 is - R2, R2 is a hydrogen atom, or an optionally substituted group bonded via a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom, and when ===R2 is =R2, R2 is an oxo group, an optionally substituted alkylidene group, or an optionally, substituted imino group.