40926-73-6

Basic information

• Product Name: (2-METHOXY-PHENOXY)-ACETYL CHLORIDE
• Synonyms: (2-METHOXY-PHENOXY)-ACETYL CHLORIDE
• CAS NO: 40926-73-6
• Molecular Formula: C₉H₉ClO₃
• Molecular Weight: 200.62
• Mol File: 40926-73-6.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2-METHOXY-PHENOXY)-ACETYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-METHOXY-PHENOXY)-ACETYL CHLORIDE(40926-73-6)
• EPA Substance Registry System: (2-METHOXY-PHENOXY)-ACETYL CHLORIDE(40926-73-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 40926-73-6(Hazardous Substances Data)

Usage

Description

(2-METHOXY-PHENOXY)-ACETYL CHLORIDE is a chlorinated acetyl derivative of 2-methoxyphenol with the chemical formula C10H11ClO3. It is a colorless to pale yellow liquid with a pungent odor and is highly reactive due to the presence of the acetyl chloride group. This reactivity makes it a valuable reagent in various chemical reactions.
Used in Pharmaceutical Industry:
(2-METHOXY-PHENOXY)-ACETYL CHLORIDE is used as a precursor in the synthesis of various pharmaceuticals. Its reactivity allows for the creation of a wide range of drug compounds, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
In the agrochemical field, (2-METHOXY-PHENOXY)-ACETYL CHLORIDE is used as a starting material for the production of various agrochemicals. Its role in the synthesis of these compounds helps to improve agricultural yields and control pests.
Used in Fine Chemicals Industry:
(2-METHOXY-PHENOXY)-ACETYL CHLORIDE is also utilized as a precursor in the synthesis of fine chemicals. Its versatility in organic synthesis allows for the production of specialty chemicals used in various applications, such as fragrances, dyes, and other industrial products.
Due to the high reactivity of (2-METHOXY-PHENOXY)-ACETYL CHLORIDE, it is crucial to handle and store it with care to prevent accidental exposure and potential hazards. Proper safety measures and equipment are recommended during its use in chemical reactions and processes.

Upstream product

• 1878-85-9 (2-methoxyphenoxy)acetic acid 
• 90-05-1 2-methoxy-phenol 
• 38768-62-6 methyl (2-methoxyphenoxy) ethanoate 

Downstream Products

• 15208-64-7 N-<2-Diazo-3-oxo-4-(2-methoxy-phenoxy)-butyryl>-glycin-aethylester 
• 75057-56-6 6,7-dibromo-2-(2-methoxy-phenoxymethyl)-benzo[d][1,3]oxazin-4-one 
• 55691-24-2 (2-Methoxy-phenoxy)-thioacetic acid S-(2-thiocyanato-ethyl) ester 
• 75057-57-7 7-iodo-2-(2-methoxy-phenoxymethyl)-benzo[d][1,3]oxazin-4-one 
• 75057-55-5 2-(2-methoxy-phenoxymethyl)-benzo[d][1,3]oxazin-4-one 
• 78961-74-7 1-Aziridin-1-yl-2-(2-methoxy-phenoxy)-ethanone 
• 79263-62-0 guaiacylmethyl chloride 
• 92197-74-5 diethyl <(2-methoxy)phenoxy>acetamide 
• 114914-30-6 2-methoxyphenoxyacetyl-cyanomethylenetriphenylphosphorane 
• 345650-01-3 [2-(2-Methoxy-phenoxymethyl)-4-oxo-4H-quinazolin-3-yl]-acetic acid 
• 15687-23-7 diethyl-[2-(2-methoxy-phenoxy)-ethyl]-amine 
• 73342-49-1 2-(2-methoxy-phenoxymethyl)-3-thiazol-2-yl-3H-quinazolin-4-one 
• 75057-65-7 7-iodo-2-(2-methoxy-phenoxymethyl)-3-thiazol-2-yl-3H-quinazolin-4-one 
• 75057-64-6 6,7-dibromo-2-(2-methoxy-phenoxymethyl)-3-thiazol-2-yl-3H-quinazolin-4-one 

Relevant articles and documents

Design and Synthesis of Novel 4-Hydroxyl-3-(2-phenoxyacetyl)-pyran-2-one Derivatives for Use as Herbicides and Evaluation of Their Mode of Action

In order to develop a novel herbicide containing the β-triketone motif, a series of 4-hydroxyl-3-(2-phenoxyacetyl)-pyran-2-one derivatives were designed and synthesized. The bioassay results showed that compound II15 had good pre-emergent herbicidal activity even at a dosage of 187.5 g ha-1. Moreover, compound II15 showed a broader spectrum of weed control when compared with a commercial herbicide 2,4-dichlorophenoxyacetic acid (2,4-D), and displayed good crop safety to Triticum aestivum L. and Zea mays Linn. when applied at 375 g ha-1 under pre-emergence conditions, which indicated its great potential as a herbicide. More importantly, studying the molecular mode of action of compound II15 revealed that the novel triketone structure is a proherbicide of its corresponding phenoxyacetic acid auxin herbicide, which has a herbicidal mechanism similar to that of 2,4-D. The present work indicates that the 4-hydroxyl-3-(2-phenoxyacetyl)-pyran-2-one motif may be a potential lead structure for further development of novel auxin-type herbicides.

Isoflavone amide derivatives, their preparation method and medical use

The invention belongs to the field of medicinal chemistry, and relates to derivatives of isoflavones amides, as well as a preparation method and medical application of derivatives, in particular to the derivatives of the isoflavones amides with the general formula of (I) shown as the specification, the preparation method and the medical application of the derivatives, particularly the application of the derivatives of the isoflavones amides serving as medicaments for preventing or treating hyperlipemia, adiposis or type-II diabetes.

Formononetin derivatives and preparation methods and medical application thereof

The invention relates to the field of pharmaceutical chemistry, and relates to formononetin derivatives and preparation methods and medical application thereof, in particular to formononetin derivatives with the general formula as shown in (I), preparation methods thereof, pharmaceutical compositions containing the compounds and medical application of the derivatives and the pharmaceutical compositions, particularly, application of the derivatives and the pharmaceutical compositions serving as drugs for preventing or treating hyperlipidaemia or obesity or type-II diabetes. Please see the formula in the description.