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16024-55-8

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16024-55-8 Usage

Description

2-(2-Methoxyethoxy)acetyl chloride, with the molecular formula C6H11ClO4, is a chlorinated derivative of ethylene glycol monoethyl ether. It is a colorless to pale yellow liquid with a pungent odor and is highly volatile. 2-(2-METHOXYETHOXY)ACETYL CHLORIDE is utilized as a reagent in organic synthesis and is known for its potential irritant and corrosive properties, necessitating careful handling and storage.

Uses

Used in Pharmaceutical Industry:
2-(2-Methoxyethoxy)acetyl chloride is used as a reagent for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to participate in a range of organic reactions, contributing to the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(2-Methoxyethoxy)acetyl chloride serves as a reagent in the production of agrochemicals. Its role in organic synthesis aids in the creation of compounds that can be used in pesticides, herbicides, and other agricultural products to enhance crop protection and yield.
Used in Dye Industry:
2-(2-Methoxyethoxy)acetyl chloride is utilized as a reagent in the synthesis of dyes. Its involvement in organic reactions facilitates the production of a variety of dyes used in different industries, including textiles, plastics, and printing inks.
Used as a Solvent in Chemical Reactions:
Beyond its role as a reagent, 2-(2-Methoxyethoxy)acetyl chloride also functions as a solvent in various chemical processes. Its properties enable it to dissolve a range of substances, making it a valuable component in numerous chemical reactions and processes.
Used as a Precursor in Organic Synthesis:
2-(2-Methoxyethoxy)acetyl chloride is employed as a precursor in the synthesis of other organic compounds. Its versatility in organic chemistry allows it to be a starting material for the creation of a multitude of organic molecules, expanding the scope of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 16024-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,2 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16024-55:
(7*1)+(6*6)+(5*0)+(4*2)+(3*4)+(2*5)+(1*5)=78
78 % 10 = 8
So 16024-55-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H9ClO3/c1-8-2-3-9-4-5(6)7/h2-4H2,1H3

16024-55-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L18423)  2-(2-Methoxyethoxy)acetyl chloride, 95%   

  • 16024-55-8

  • 1g

  • 429.0CNY

  • Detail
  • Alfa Aesar

  • (L18423)  2-(2-Methoxyethoxy)acetyl chloride, 95%   

  • 16024-55-8

  • 5g

  • 1536.0CNY

  • Detail

16024-55-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-METHOXYETHOXY)ACETYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 2-methoxyethoxy acetyl chloride

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:16024-55-8 SDS

16024-55-8Downstream Products

16024-55-8Relevant articles and documents

Polycyclic compounds from aminopolyols and a-dicarbonyls: Structure and application in the synthesis of exoditopic ligands

Giovenzana, Giovanni B.,Palmisano, Giovanni,Del Grosso, Erika,Giovannelli, Lorella,Penoni, Andrea,Pilati, Tullio

, p. 1489 - 1494 (2005)

The structure and stereochemistry of the crystalline 2 : 2 condensation product ("glytham") of glyoxal and tris(hydroxymethyl)aminomethane was conclusively determined by X-ray diffractometric analysis. The singular disposition of the heteroatoms suggests the employment of glytham as starting material for the synthesis of ditopic ligands for metal ions. Some derivatives of glytham were prepared and their binding properties towards alkaline metal ions were preliminarily investigated by ESI-MS and NMR. The Royal Society of Chemistry 2005.

IMIDAZOTHIADIAZOLE AND IMIDAZOPYRAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION

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Paragraph 00155, (2013/11/18)

The present invention provides thiazole compounds of Formula I wherein W, Y, R0, R2, R4, R5, R6, R7, X1, X2, X3 and X4 are as defined herein, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are inhibitors of platelet aggregation and thus can be used as medicaments for treating or preventing thromboembolic disorders.

SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES WITH A CHAIN EXTENSION

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Page/Page column 25, (2008/06/13)

The invention relates to substituted cyclohexyl-1,4-diamine derivatives, to a method for their production, to medicaments containing said compounds and to the use of substituted cyclohexyl-1,4-diamine derivatives for producing medicaments.

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