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2-Chloro-N-methoxy-N-methylacetamide is an organic compound that serves as a key intermediate in the synthesis of various biologically active molecules. It is characterized by its unique structure, which includes a chloro, methoxy, and methyl groups attached to an amide functional group.
Used in Pharmaceutical Industry:
2-Chloro-N-methoxy-N-methylacetamide is used as a starting reagent for the one-pot synthesis of 2-heptyl-3-hydroxy-4(1H)-quinolone (PQS), a signaling molecule involved in the quorum sensing of Pseudomonas aeruginosa. This application is crucial for the development of new drugs targeting bacterial communication and virulence.
Used in Chemical Synthesis:
2-Chloro-N-methoxy-N-methylacetamide is used as an intermediate in the preparation of 2-alkyl-4-quinolones, a class of compounds with significant biological activity. These quinolones have potential applications in various fields, including medicine and agriculture, due to their antimicrobial and antifungal properties.
Used in Research and Development:
2-Chloro-N-methoxy-N-methylacetamide is utilized in the synthesis of 2-(benzo[d]thiazol-2-ylsulfonyl)-N-methoxy-N-methylacetamide and α-chloro-ketone, which are valuable compounds for further research and development in the field of organic chemistry. These compounds can be used to explore new synthetic routes and develop novel molecules with potential applications in various industries.

67442-07-3

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67442-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67442-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,4 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67442-07:
(7*6)+(6*7)+(5*4)+(4*4)+(3*2)+(2*0)+(1*7)=133
133 % 10 = 3
So 67442-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H8ClNO2/c1-6(8-2)4(7)3-5/h3H2,1-2H3

67442-07-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L17048)  2-Chloro-N-methoxy-N-methylacetamide, 98%   

  • 67442-07-3

  • 5g

  • 746.0CNY

  • Detail
  • Alfa Aesar

  • (L17048)  2-Chloro-N-methoxy-N-methylacetamide, 98%   

  • 67442-07-3

  • 25g

  • 2470.0CNY

  • Detail

67442-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-N-methoxy-N-methylacetamide

1.2 Other means of identification

Product number -
Other names 2-CHLORO-N-METHOXY-N-METHYLACETAMIDE

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:67442-07-3 SDS

67442-07-3Relevant academic research and scientific papers

Substituted Tetraethynylethylene–Tetravinylethylene Hybrids

Connor, Kieran P. E.,Horvath, Kelsey L.,Magann, Nicholas L.,Sherburn, Michael S.,Sowden, Madison J.,Westley, Erin

supporting information, p. 977 - 986 (2022/02/03)

A general synthetic approach to molecular structures that are hybrids of tetraethynylethylene (TEE) and tetravinylethylene (TVE) is reported. The synthesis permits the controlled preparation of many previously inaccessible structures, including examples w

Development of a practical synthesis to PI3K α-selective inhibitor GDC-0326

Koenig, Stefan G.,Green, Keena L.,Müller, Barbara,Sowell, C. Gregory,Askin, David,Gosselin, Francis

, (2020/12/29)

A practical route to PI3K α-selective inhibitor GDC-0326 is reported. The synthesis leverages an existing scheme to a key tetracyclic benzoxazepine intermediate and optimizes it for robustness and scalability, including removing numerous undesired conditions and reagents, as well as eliminating chromatographic purification steps. The process endgame is streamlined to utilize a single-step, stereocontrolled alkylation of the key phenol with a chiral lactamide mesylate, followed by recrystallization of the lactamide ether product, to deliver the desired enantiomer of the active pharmaceutical ingredient (API) GDC-0326.

Concise and Efficient Synthesis of [6]-Paradol

Shi, Xiang,Xia, Tiantian,McKamey, Brooke E.,Wu, Xian,Sun, Yue,Zhou, Weifeng,Zhang, Guangyan

, p. 1360 - 1365 (2021/06/21)

An efficient synthesis of [6]-paradol (1) has been performed in four steps with a 72.0% overall yield. The present method highlights commercially available materials, convenient isolation with multiple crystallization without involving column chromatography, and a high-purity product (more than 99.2%), and it is amenable to large-scale synthesis.

3-SUBSTITUTED PHENYLAMIDINE COMPOUNDS, PREPARATION AND USE THEREOF

-

Paragraph 0389-0390, (2021/10/14)

The present invention discloses 3 - substituted anilino compounds of formula (I) in which R 1, R 2, R 3, R 4, R 44a, R 44b, A and E are as defined in the description. The present invention further discloses processes for preparing compounds of general formula (I) and using compounds of general formula (I) as crop protection agents for agricultural crops.

Quaternary Charge-Transfer Complex Enables Photoenzymatic Intermolecular Hydroalkylation of Olefins

Page, Claire G.,Cooper, Simon J.,Dehovitz, Jacob S.,Oblinsky, Daniel G.,Biegasiewicz, Kyle F.,Antropow, Alyssa H.,Armbrust, Kurt W.,Ellis, J. Michael,Hamann, Lawrence G.,Horn, Evan J.,Oberg, Kevin M.,Scholes, Gregory D.,Hyster, Todd K.

supporting information, p. 97 - 102 (2021/01/12)

Intermolecular C-C bond-forming reactions are underdeveloped transformations in the field of biocatalysis. Here we report a photoenzymatic intermolecular hydroalkylation of olefins catalyzed by flavin-dependent 'ene'-reductases. Radical initiation occurs via photoexcitation of a rare high-order enzyme-templated charge-transfer complex that forms between an alkene, α-chloroamide, and flavin hydroquinone. This unique mechanism ensures that radical formation only occurs when both substrates are present within the protein active site. This active site can control the radical terminating hydrogen atom transfer, enabling the synthesis of enantioenriched γ-stereogenic amides. This work highlights the potential for photoenzymatic catalysis to enable new biocatalytic transformations via previously unknown electron transfer mechanisms.

Paradol synthesis method

-

Paragraph 0032; 0038, (2020/04/17)

The invention discloses a complete synthesis method of a natural product paradol, the route being represented as the specification. The method employs feasible raw materials and simple operation, is high in yield and low in cost, is high in final product purity, is controllable in quality, and is suitable for industrial production.

PESTICIDAL MIXTURES COMPRISING A MESOIONIC COMPOUND

-

Page/Page column 48; 51; 52, (2020/04/25)

Pesticidal mixtures comprising as active compounds 1) pesticidally active compound A of formula (I) and 2) at least one further compound B selected from compounds B1 to B22 as described in claims and the description.

PYRIMIDINIUM COMPOUNDS AND THEIR MIXTURES FOR COMBATING ANIMAL PESTS

-

Paragraph 0386; 0403, (2020/07/31)

The present invention relates to pyrimidinium compounds of formula (I), to the stereoisomers, salts, tautomers and N-oxides thereof, their mixtures and to compositions comprising such compounds or mixtures. The invention also relates to methods and uses o

METHOD OF CONTROLLING RICE PESTS IN RICE

-

Paragraph 0154; 0155, (2020/09/22)

The present invention relates to methods for controlling rice pest invertebrates, which methods comprise applying pyrimidinium compounds of formula (I), the stereoisomers, salts, tautomers and N-oxides thereof, their mixtures and compositions comprising such compounds or mixtures, by seedling box application.

PROCESS FOR PREPARING S-CONTAINING PYRIMIDINIUM COMPOUNDS

-

Paragraph 0318-0319, (2020/08/18)

The present invention relates to a process for preparing optically active compounds of formula X and intermediates thereof, wherein the variables of compound of formula X are as defined in the claims and the description.

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