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

• 110-91-8 morpholine 
• 625-99-0 3-iodochlorobenzene 
• 5765-65-1 4-(benzoyloxy)morpholine 
• 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 
• 108-42-9 3-chloro-aniline 
• 7519-92-8 tris(3-chlorophenyl)boroxine 
• 637-87-6 1-Chloro-4-iodobenzene 
• 106-39-8 bromochlorobenzene 
• 541-73-1 1,3-Dichlorobenzene 

Downstream Products

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

Relevant articles and documents

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

Photo-induced dealdehyding method

The invention provides a photo-induced dealdehyding method, and belongs to the technical field of organic synthesis. The photo-induced dealdehyding method comprises the following steps that a mixtureof a compound shown in the formula I and a solvent are reacted under an inert gas atmosphere and visible light irradiation, a dealdehyding product is obtained, and no photocatalyst is used in the whole process; wherein the structural formula of the formula I shown in the specification, R is a functional group and is selected from hydrogen, methyl, methoxyl, cyano, chlorine, bromine or fluorine. According to the photo-induced dealdehyding method, in the inert gas atmosphere, the compound shown in the formula (I) can be excited to generate carbon-oxygen bond homogeneous cracking through visiblelight irradiation, then free radical migration and double bond displacement are conducted, finally carbon monoxide is removed, aldehyde group removal is completed, no photocatalyst is needed in the whole process, operation is easy and convenient, and conditions are mild.

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