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19202-04-1

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19202-04-1 Usage

Description

(4-Chlorophenyl)(morpholino)methanone, a chemical compound with the molecular formula C11H12ClNO2, is a white to off-white solid. It features a morpholine ring attached to a phenyl group, which is substituted with a chlorine atom and a ketone functional group. (4-Chlorophenyl)(morpholino)methanone is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, serving as a building block in organic synthesis for various industrial applications. Due to its potential to cause skin and eye irritation, it should be handled with care and stored in a cool, dry place away from direct sunlight and heat sources.

Uses

Used in Pharmaceutical Industry:
(4-Chlorophenyl)(morpholino)methanone is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, potentially leading to the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (4-Chlorophenyl)(morpholino)methanone serves as a precursor in the production of agrochemicals. Its incorporation into these products can contribute to the development of more effective and targeted pest control solutions.
Used in Organic Synthesis:
(4-Chlorophenyl)(morpholino)methanone is utilized as a building block in organic synthesis, enabling the creation of a wide range of chemical compounds for various industrial applications. Its versatility in chemical reactions makes it a valuable component in the synthesis of specialty chemicals and other complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 19202-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,0 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19202-04:
(7*1)+(6*9)+(5*2)+(4*0)+(3*2)+(2*0)+(1*4)=81
81 % 10 = 1
So 19202-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClNO2/c12-10-3-1-9(2-4-10)11(14)13-5-7-15-8-6-13/h1-4H,5-8H2

19202-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Chlorobenzoyl)morpholine

1.2 Other means of identification

Product number -
Other names (4-chlorophenyl)-morpholin-4-ylmethanone

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:19202-04-1 SDS

19202-04-1Relevant articles and documents

NaI-mediated oxidative amidation of benzyl alcohols/aromatic aldehydes to benzamides via electrochemical reaction

Rerkrachaneekorn, Tanawat,Tankam, Theeranon,Sukwattanasinitt, Mongkol,Wacharasindhu, Sumrit

supporting information, (2021/04/15)

In this research, we have developed a mild electrochemical process for oxidative amidation of benzyl alcohols/aromatic aldehydes with cyclic amines into the corresponding benzamides. This electroorganic synthetic method proceeds using NaI as a redox mediator under ambient temperature in undivided cell, providing more than 25 examples of amide products in moderate to good yields. The benefits of this reaction include one-pot synthesis, open air condition, proceed in aqueous media and no requirement of external conducting salt, base and oxidant.

Solar and visible-light active nano Ni/g-C3N4photocatalyst for carbon monoxide (CO) and ligand-free carbonylation reactions

Hosseini-Sarvari, Mona,Akrami, Zahra

, p. 956 - 969 (2021/02/26)

In this study, we investigate the amino and alkoxycarbonylation reaction between various substituted aryl halides, benzyl iodides, and iodocyclohexane with different types of amines and alcohols in the absence of carbon monoxide gas and ligands. Similar reactions are carried out at high temperatures, in the presence of appropriate ligands, stoichiometric amounts of bases, and gaseous carbon monoxide, which endanger the health of organic chemists. We present a novel method that does not utilize ligands, bases, gaseous CO, and special conditions. This procedure is a redox reaction carried out by new economic nano Ni/g-C3N4at room temperature and under visible light. Mo(CO)6was used toin situgenerate CO, to resolve the problems caused by the use of CO gas. This protocol has the ability to be used on a gram scale by using a continuous flow reactor.

Method for preparing amide from carboxylic acid under irradiation of blue light by taking iridium and cobalt complexes as catalysts

-

Paragraph 0041-0042, (2021/05/12)

The invention relates to a method for preparing amide from carboxylic acid under the irradiation of blue light by taking iridium and cobalt complexes as catalysts, and belongs to the field of chemistry. The method comprises the following step of: by taking R substituted carboxylic acid and R1' and R2' substituted amines as raw materials, triphenylphosphine as a deoxidizing agent, [Ir(dF(CF3)ppy)2(dtbbpy)]PF6 as a photocatalyst and Co(dmgH)(dmgH2)Cl2 as a metal complex catalyst, reacting in dichloromethane in an inert atmosphere and under the irradiation of blue light to obtain an amide compound, wherein R is an aryl group, a heteroaryl group, a protected amino group, a substituted alkyl group, a substituted aryl group or a substituted protected amino group, R1' is a hydrogen group, a substituted alkyl group, a phenyl group or a substituted phenyl group, and R2' is a hydrogen group, a substituted alkyl group, a phenyl group or a substituted phenyl group.

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