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122334-37-6

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122334-37-6 Usage

Description

4-Chloro-N-methoxy-N-methylacetamide is a chemical compound that belongs to the class of amides. It is characterized by the presence of a chlorine atom at the 4-position, a methoxy group, and a methyl group attached to the nitrogen atom. 4-Chloro-N-methoxy-N-methylacetamide is a derivative of Ketamine, which is an intravenous anesthetic.

Uses

Used in Pharmaceutical Industry:
4-Chloro-N-methoxy-N-methylacetamide is used as an anesthetic agent for its ability to induce a state of pain relief and sedation. It is particularly useful in medical procedures that require intravenous anesthesia, providing a safe and effective means of managing pain and discomfort during surgery or other medical interventions.
Additionally, due to its structural similarity to Ketamine, 4-Chloro-N-methoxy-N-methylacetamide may also have potential applications in the development of new anesthetic drugs or in the study of the mechanisms of action of existing anesthetic agents. This could lead to the discovery of more effective and safer anesthetics for various medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 122334-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,3 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 122334-37:
(8*1)+(7*2)+(6*2)+(5*3)+(4*3)+(3*4)+(2*3)+(1*7)=86
86 % 10 = 6
So 122334-37-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10ClNO2/c1-11(13-2)9(12)7-3-5-8(10)6-4-7/h3-6H,1-2H3

122334-37-6SDS

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-chloro-N-methoxy-N-methylbenzamide

1.2 Other means of identification

Product number -
Other names 4-chloro-N-methoxy-N-methyl-benzamide

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:122334-37-6 SDS

122334-37-6Relevant articles and documents

Rhoda-Electrocatalyzed Bimetallic C?H Oxygenation by Weak O-Coordination

Tan, Xuefeng,Massignan, Leonardo,Hou, Xiaoyan,Frey, Johanna,Oliveira, Jo?o C. A.,Hussain, Masoom Nasiha,Ackermann, Lutz

supporting information, p. 13264 - 13270 (2021/05/06)

Rhodium-electrocatalyzed arene C?H oxygenation by weakly O-coordinating amides and ketones have been established by bimetallic electrocatalysis. Likewise, diverse dihydrooxazinones were selectively accessed by the judicious choice of current, enabling twofold C?H functionalization. Detailed mechanistic studies by experiment, mass spectroscopy and cyclovoltammetric analysis provided support for an unprecedented electrooxidation-induced C?H activation by a bimetallic rhodium catalysis manifold.

Phase-Transfer Catalyzed Asymmetric [4 + 1] Annulations for the Synthesis of Chiral 2,2-Disubstituted Tetrahydrothiophenes

Yin, Qi,Wen, Xiaolu,Chen, Yiwei,Gong, Xiangnan,Hu, Lin

supporting information, p. 7529 - 7534 (2021/10/02)

An efficient catalytic asymmetric [4 + 1] reaction, which features the use of simple β-keto esters as one-carbon nucleophiles and 5-succinimidothio-pent-2-enoates as four-atom bielectrophiles, has been developed in the presence of a bifunctional chiral ph

Iron-Catalyzed, Iminyl Radical-Triggered Cascade 1,5-Hydrogen Atom Transfer/(5+2) or (5+1) Annulation: Oxime as a Five-Atom Assembling Unit

Chen, Ying-Chun,Du, Fei,Jiang, Kun,Liang, Wu,Ouyang, Qin,Shuai, Li,Wei, Ye,Yang, Jie

supporting information, p. 19222 - 19228 (2020/08/25)

By integration of iminyl radical-triggered 1,5-hydrogen atom transfer and (5+2) or (5+1) annulation processes, a series of structurally novel and interesting azepine and spiro-tetrahydropyridine derivatives have been successfully prepared in moderate to good yields. This method utilizes FeCl2 as the catalyst and readily available oximes as five-atom units, while showcasing broad substrate scope and good functional group compatibility. The annulation products can be easily converted into many valuable compounds. Moreover, DFT calculation studies are performed to provide some insights into the possible reaction mechanisms for the (5+2) and (5+1) annulations.

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