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122439-14-9

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122439-14-9 Usage

General Description

4-(3-Methoxy-benzyl)-morpholine is a chemical compound that has the molecular formula C13H19NO2. It is a morpholine derivative with a 3-methoxybenzyl substitution at the 4-position. 4-(3-METHOXY-BENZYL)-MORPHOLINE is commonly used in the pharmaceutical industry as a building block for the synthesis of various bioactive molecules and pharmaceutical drugs. It is also used as a reagent in organic synthesis and chemical research. 4-(3-Methoxy-benzyl)-morpholine has the potential to exhibit various biological activities and may have applications in medicinal chemistry and drug development due to its structural features and potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 122439-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,3 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122439-14:
(8*1)+(7*2)+(6*2)+(5*4)+(4*3)+(3*9)+(2*1)+(1*4)=99
99 % 10 = 9
So 122439-14-9 is a valid CAS Registry Number.

122439-14-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(3-methoxyphenyl)methyl]morpholine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:122439-14-9 SDS

122439-14-9Relevant articles and documents

Electrochemical Activation of Diverse Conventional Photoredox Catalysts Induces Potent Photoreductant Activity**

Chernowsky, Colleen P.,Chmiel, Alyah F.,Wickens, Zachary K.

supporting information, p. 21418 - 21425 (2021/08/25)

Herein, we disclose that electrochemical stimulation induces new photocatalytic activity from a range of structurally diverse conventional photocatalysts. These studies uncover a new electron-primed photoredox catalyst capable of promoting the reductive cleavage of strong C(sp2)?N and C(sp2)?O bonds. We illustrate several examples of the synthetic utility of these deeply reducing but otherwise safe and mild catalytic conditions. Finally, we employ electrochemical current measurements to perform a reaction progress kinetic analysis. This technique reveals that the improved activity of this new system is a consequence of an enhanced catalyst stability profile.

Thiourea-Catalyzed C?F Bond Activation: Amination of Benzylic Fluorides

Houle, Camille,Savoie, Paul R.,Davies, Clotilde,Jardel, Damien,Champagne, Pier Alexandre,Bibal, Brigitte,Paquin, Jean-Fran?ois

, p. 10620 - 10625 (2020/07/24)

We describe the first thiourea-catalyzed C?F bond activation. The use of a thiourea catalyst and Ti(OiPr)4 as a fluoride scavenger allows the amination of benzylic fluorides to proceed in moderate to excellent yields. Preliminary results with S- and O-based nucleophiles are also presented. DFT calculations reveal the importance of hydrogen bonds between the catalyst and the fluorine atom of the substrate to lower the activation energy during the transition state.

Base-promoted N-alkylation using formamides as the N-sources in neat water

Chen, Wen-Xin,Zhang, Cai-Yun,Shao, Li-Xiong

, p. 880 - 885 (2014/01/23)

An efficient catalyst-free, alternative method for the C-N bond formation reaction of alkyl electrophiles using formamides as the N-sources was achieved under mild conditions. The reaction possesses the advantages of a broad range of substrates scope and wide functional group tolerance. It should also be noted that this process was performed using the environmentally benign water as the sole solvent, and high yield can also be achieved in ten-gram scale.

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