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3'-CHLORO-2'-FLUOROACETOPHENONE, with the chemical formula C8H6ClFO, is a white solid chemical compound characterized by a strong odor. It is soluble in organic solvents and is recognized for its reactivity, which necessitates careful handling due to its potential toxicity and irritating properties. 3'-CHLORO-2'-FLUOROACETOPHENONE serves as a versatile intermediate in the synthesis of a variety of organic compounds, including pharmaceuticals and agrochemicals, and is utilized as a building block for the creation of aromatic and heterocyclic compounds.

161957-59-1

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161957-59-1 Usage

Uses

Used in Pharmaceutical Synthesis:
3'-CHLORO-2'-FLUOROACETOPHENONE is used as a key intermediate in the production of pharmaceuticals for its ability to contribute to the development of new medications with specific therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 3'-CHLORO-2'-FLUOROACETOPHENONE is employed as an intermediate, playing a crucial role in the synthesis of compounds designed to protect crops and enhance agricultural productivity.
Used in Organic Compounds Synthesis:
3'-CHLORO-2'-FLUOROACETOPHENONE is used as a building block in the synthesis of various aromatic and heterocyclic compounds, which are essential in a wide range of applications across different industries.
Used in Research Laboratories:
3'-CHLORO-2'-FLUOROACETOPHENONE is a common feature in research laboratories where it is used for experimental purposes, contributing to the advancement of chemical knowledge and the development of new chemical processes or products.
Used in Chemical Synthesis Industries:
3'-CHLORO-2'-FLUOROACETOPHENONE is utilized in the chemical synthesis industry as a reactive intermediate, essential for the large-scale production of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 161957-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,5 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 161957-59:
(8*1)+(7*6)+(6*1)+(5*9)+(4*5)+(3*7)+(2*5)+(1*9)=161
161 % 10 = 1
So 161957-59-1 is a valid CAS Registry Number.

161957-59-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H26474)  3'-Chloro-2'-fluoroacetophenone, 96%   

  • 161957-59-1

  • 1g

  • 413.0CNY

  • Detail
  • Alfa Aesar

  • (H26474)  3'-Chloro-2'-fluoroacetophenone, 96%   

  • 161957-59-1

  • 5g

  • 1274.0CNY

  • Detail
  • Alfa Aesar

  • (H26474)  3'-Chloro-2'-fluoroacetophenone, 96%   

  • 161957-59-1

  • 25g

  • 4007.0CNY

  • Detail

161957-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Chloro-2-fluorophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 3′-Chloro-2′-fluoroacetophenone

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:161957-59-1 SDS

161957-59-1Relevant academic research and scientific papers

Lithiations directed by carboxylic acid, fluorine and chlorine: The regioselective synthesis of polysubstituted benzoic acids and acetophenones

Moyroud, Joel,Guesnet, Jean-Luc,Bennetau, Bernard,Mortier, Jacques

, p. 133 - 141 (2007/10/03)

Lithiation/electrophilic quenching of ortho-lithiated benzoates allows the totally regiocontrolled synthesis of a wide range of 2,3-, 2,3,4-, and 2,3,4,5-polysubstituted benzoic acids and related acetophenones. Elsevier,.

Regiospecific Synthesis of Mixed 2,3-Dihalobenzoic Acids and Related Acetophenones via Ortho-Metalation Reactions

Moyroud, Joel,Guesnet, Jean-Luc,Bennetau, Bernard,Mortier, Jacques

, p. 881 - 884 (2007/10/02)

Concise general routes to mixed 2,3-dihalobenzoic acids and related acetophenones-based on directed ortho-metalation and ipso-desilylation reactions are described.

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