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826990-47-0

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826990-47-0 Usage

Description

(3-chloro-4-fluorophenoxy)acetyl chloride is a chemical compound with the molecular formula C8H6ClFO2. It is a derivative of acetyl chloride and contains a phenyl ring with a chlorine atom at the 3-position and a fluorine atom at the 4-position. The acetyl group is attached to the phenyl ring via an oxygen atom.

Uses

Used in Organic Synthesis:
(3-chloro-4-fluorophenoxy)acetyl chloride is used as a reagent for the introduction of the (3-chloro-4-fluorophenoxy)acetyl group into various organic molecules. This allows for the creation of new compounds with specific properties and functions.
Used in Pharmaceutical Production:
(3-chloro-4-fluorophenoxy)acetyl chloride is used as an intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Production:
(3-chloro-4-fluorophenoxy)acetyl chloride is used in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties make it suitable for the development of effective and targeted agricultural products.
Used in Polymer Manufacturing:
(3-chloro-4-fluorophenoxy)acetyl chloride is used in the manufacturing of polymers. Its incorporation into polymer structures can enhance their properties, such as strength, stability, and resistance to environmental factors.
Used in Other Industrial Processes:
(3-chloro-4-fluorophenoxy)acetyl chloride has applications in various industrial processes, where its unique chemical properties can be utilized for specific purposes, such as in the production of specialty chemicals or materials.

Check Digit Verification of cas no

The CAS Registry Mumber 826990-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,6,9,9 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 826990-47:
(8*8)+(7*2)+(6*6)+(5*9)+(4*9)+(3*0)+(2*4)+(1*7)=210
210 % 10 = 0
So 826990-47-0 is a valid CAS Registry Number.

826990-47-0SDS

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-(3-chloro-4-fluorophenoxy)acetyl chloride

1.2 Other means of identification

Product number -
Other names 3-chloro-4-fluoro-phenoxyacetyl 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:826990-47-0 SDS

826990-47-0Relevant articles and documents

NOVEL PYRIDOPYRIMIDINONE COMPOUNDS FOR MODULATING THE CATALYTIC ACTIVITY OF HISTONE LYSINE DEMETHYLASES (KDMS)

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Page/Page column 167, (2016/05/19)

The present invention provides a compound of Formula (I) being capable of modulating the activity of histone lysine demethylase (KDM), pharmaceutical compositions thereof, methods to prepare the said compounds, and the use of such compounds as a medicament. The compound of Formula (I) acts as KDM inhibitor with marked potency, thereby having an outstanding potential for a pharmaceutical intervention of cancer and any other diseases related to KDM dysregulation.

One-pot synthesis of fluorine containing 3-cyano/ethoxycarbonyl-2-methyl- benzo[b]furans

RamaRao,Venkat Reddy,Maitraie,Ravikanth,Yadla,Narsaiah,Shanthan Rao

, p. 12231 - 12237 (2007/10/03)

Fluoro-substituted 3-cyano-2-methyl-benzo[b]furans and ethyl 2-methyl-benzo[b]furan-3-carboxylates are conveniently prepared in a single step in good yield by the microwave induced tandem intramolecular Wittig and Claisen rearrangement reactions of the corresponding [(aryloxyacetyl) (cyano) methylene] triphenylphosphorane and [(aryloxyacetyl) (ethoxycarbonyl) methylene] triphenylphosphoranes, respectively. Graphical Abstract

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