41605-90-7

Basic information

• Product Name: 4-(3-Chlorophenyl)morpholine
• Synonyms: 4-(3-Chlorophenyl)morpholine;N-(m-Chlorophenyl)morpholine
• CAS NO: 41605-90-7
• Molecular Formula: C₁₀H₁₂ClNO
• Molecular Weight: 197.66
• Product Categories: pharmacetical
• Mol File: 41605-90-7.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 324°Cat760mmHg
• Flash Point: 149.8°C
• Appearance: /
• Density: 1.2g/cm³
• Vapor Pressure: 0.000252mmHg at 25°C
• Refractive Index: 1.556
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-(3-Chlorophenyl)morpholine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-Chlorophenyl)morpholine(41605-90-7)
• EPA Substance Registry System: 4-(3-Chlorophenyl)morpholine(41605-90-7)

Safety Data

• Hazardous Substances Data: 41605-90-7(Hazardous Substances Data)

Usage

General Description

4-(3-Chlorophenyl)morpholine is a chemical compound consisting of functional groups such as morpholine and chlorophenyl. 4-(3-Chlorophenyl)morpholine is often used in scientific research and is known for its ability to serve as a building block in the development of various pharmaceuticals and synthetic organic compounds. Its exact properties will largely depend on the conditions under which it is used, the purity and the other substances with which it comes into contact.

InChI:InChI=1/C10H12ClNO/c11-9-2-1-3-10(8-9)12-4-6-13-7-5-12/h1-3,8H,4-7H2

Upstream product

• 1708-29-8 2,5-dihydrofuran 
• 108-42-9 3-chloro-aniline 
• 5765-65-1 4-(benzoyloxy)morpholine 
• 7519-92-8 tris(3-chlorophenyl)boroxine 
• 615-41-8 2-iodochlorobenzene 
• 61072-56-8 4-chloro-2-fluorobenzaldehyde 
• 387-45-1 2-chloro-6-fluorobenzaldehyde 
• 68415-31-6 2-chloro-6-(morpholin-4-yl)benzaldehyde 
• 109-02-4 4-methyl-morpholine 
• 34604-52-9 diethylene glycol dimesylate 
• 110-91-8 morpholine 
• 625-99-0 3-iodochlorobenzene 
• 637-87-6 1-Chloro-4-iodobenzene 
• 106-39-8 bromochlorobenzene 

Downstream Products

• 28276-89-3 2-(N-(3-chlorophenyl)formamido)ethyl formate 

Relevant articles and documents

Catalyst-free photodecarbonylation ofortho-amino benzaldehyde

It is almost a consensus that decarbonylation of the aldehyde group (-CHO) needs to not only be mediated by transition metal catalysts, but also requires severe reaction conditions (high temperature and long reaction time). In this work, inspired by the “conformational-selectivity-based” design strategy, we broke this consensus and discovered a catalyst-free photodecarbonylation of the aldehyde group. It revealed that decarbonylation can be easily achieved with visible light irradiation by introducing a tertiary amine into theortho-position of the aldehyde group. A diverse array of tertiary amines is tolerated by our photodecarbonylation under mild conditions. Furthermore, the (QM) computations of the mechanism and the experiments on well-designed special substrates revealed that our photodecarbonylation depends on the conformational specificity of the aldehyde group and tertiary amine, and occurs through an unusual [1,4]-H shift and a subsequent [1,3]-H shift.

N-heterocyclic carbene-Pd(II)-2-methyl-4,5-dihydrooxazole complex-catalyzed highly chemoselective mono-amination of dichlorobenzenes

The palladium-catalyzed chemoselective mono-amination of dichlorobenzenes was reported in this paper. Under the suitable conditions, all reactions involving the three isomers of dichlorobenzenes with various secondary and primary amines in the presence of

Three-Component Reactions of Arynes, Amines, and Nucleophiles via a One-Pot Process

An unprecedented three-component reaction of arynes, tertiary amines, and nucleophiles has been demonstrated through ammonium salt intermediates. This protocol allows access to tertiary aniline derivatives containing the piperazine motif in good-to-excell