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2-chloro-1-(2,3-difluorophenyl)ethanone is a fluoroacetophenone derivative with a chloro substituent, characterized by the molecular formula C8H6ClF2O. It is a colorless liquid with a distinctive odor and is recognized for its role as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries.

929249-82-1

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929249-82-1 Usage

Uses

Used in Pharmaceutical Industry:
2-chloro-1-(2,3-difluorophenyl)ethanone serves as a crucial intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of a wide range of medicinal compounds with diverse applications in healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 2-chloro-1-(2,3-difluorophenyl)ethanone is utilized as an intermediate for the production of various agrochemicals, including pesticides and herbicides. Its incorporation into these products helps enhance their effectiveness in controlling pests and weeds, thereby supporting agricultural productivity.
Used as a Building Block in Organic Synthesis:
Beyond its applications in pharmaceuticals and agrochemicals, 2-chloro-1-(2,3-difluorophenyl)ethanone also functions as a versatile building block in the synthesis of a variety of organic compounds. Its reactivity and structural features make it a valuable component in the creation of complex organic molecules for various industrial and research purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 929249-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,2,4 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 929249-82:
(8*9)+(7*2)+(6*9)+(5*2)+(4*4)+(3*9)+(2*8)+(1*2)=211
211 % 10 = 1
So 929249-82-1 is a valid CAS Registry Number.

929249-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(2,3-difluorophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-chloro-2',3'-difluoroacetophenone

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:929249-82-1 SDS

929249-82-1Relevant academic research and scientific papers

FLUOROPHENYL BETA-HYDROXYETHYLAMINES AND THEIR USE IN THE TREATMENT OF HYPERGLYCAEMIA

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Page/Page column 62; 63, (2019/04/11)

There is herein provided a compound of formula (I).

Process for the preparation of Caprolactam Cgrp Antagonist

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Page/Page column 4; 10, (2009/05/28)

An efficient syntheses for the preparation of (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one.

One-step synthesis of α-Chloro acetophenones from acid chlorides and Aryl precursors

Rosen, Jonathan,Steinhuebel, Dietrich,Palucki, Michael,Davies, Ian

, p. 667 - 669 (2008/02/05)

A direct and efficient method was developed for the preparation of a variety of substituted acetophenone derivatives from readily available arene precursors and acid chlorides. This method has significant generality and affords access to substitution patt

PROCESS FOR THE PREPARATION OF CGRP ANTAGONIST

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Page/Page column 8; 24, (2008/06/13)

An efficient synthesis for the preparation of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine -1-carboxamide, by coupling (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one and 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine dihydrochloride with 1,1''-carbonyldiimidazole (""CDI"") as carbonyl source; and an efficient preparation of the potassium salt of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine -1-carboxamide.

PROCESS FOR THE PREPARATION OF PYRIDINE HETEROCYCLE CGRP ANTAGONIST INTERMEDIATE

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Page/Page column 8; 24-25, (2008/06/13)

An efficient syntheses for the preparation of the intermediate 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine dihydrochloride, and other salt forms of 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine.

CGRP ANTAGONIST SALT

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Page/Page column 7; 20, (2008/06/13)

An efficient synthesis for the preparation of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine -1-carboxamide, by coupling (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one and 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine dihydrochloride with 1,1'-carbonyldiimidazole ("CDI") as carbonyl source; an efficient preparation of the potassium salt of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine -1-carboxamide; efficient syntheses for the preparation of intermediates (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one and 2-oxo-1-(4-piperidinyl)-2,3-dihydro-1H-imidazo[4,5-b]pyridine dihydrochloride, and the potassium salt of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine -1-carboxamide including the potassium salt ethanolate and potassium salt hydrate.

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