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2-Chloroethyl 4-Fluorophenyl Sulfone is a chemical compound that belongs to the sulfone group, characterized by a sulfur atom bonded to two oxygen atoms. It is known for its roles in scientific research and various industrial applications. 2-CHLOROETHYL 4-FLUOROPHENYL SULFONE is composed of fluorine, chlorine, sulfur, and other elements in its molecular structure, with chloroethyl and fluorophenyl groups attached, indicating its potential use in organic synthesis or as a building block in pharmaceuticals. Careful handling is required due to potential health and environmental risks, and specific properties such as boiling point, toxicity, and reactivity can be found in comprehensive chemical databases or material safety data sheets.

33330-46-0

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33330-46-0 Usage

Uses

Used in Scientific Research:
2-Chloroethyl 4-Fluorophenyl Sulfone is used as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure and composition make it a valuable subject for investigation.
Used in Pharmaceutical Industry:
2-Chloroethyl 4-Fluorophenyl Sulfone is used as a building block in the synthesis of pharmaceuticals. Its presence in the molecular structure of certain drugs can contribute to their therapeutic effects and properties.
Used in Organic Synthesis:
2-Chloroethyl 4-Fluorophenyl Sulfone is used as an intermediate in the synthesis of various organic compounds. Its reactivity and structural features make it a useful component in the creation of new molecules with desired properties.
Used in Industrial Applications:
2-Chloroethyl 4-Fluorophenyl Sulfone is used in various industrial processes, where its chemical properties can be harnessed for specific purposes. Its versatility and potential for modification make it a valuable asset in the development of new products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 33330-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,3 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33330-46:
(7*3)+(6*3)+(5*3)+(4*3)+(3*0)+(2*4)+(1*6)=80
80 % 10 = 0
So 33330-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClFO2S/c9-5-6-13(11,12)8-3-1-7(10)2-4-8/h1-4H,5-6H2

33330-46-0 Well-known Company Product Price

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  • Alfa Aesar

  • (A16930)  2-Chloroethyl 4-fluorophenyl sulfone, 98%   

  • 33330-46-0

  • 1g

  • 306.0CNY

  • Detail
  • Alfa Aesar

  • (A16930)  2-Chloroethyl 4-fluorophenyl sulfone, 98%   

  • 33330-46-0

  • 5g

  • 1232.0CNY

  • Detail

33330-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloroethylsulfonyl)-4-fluorobenzene

1.2 Other means of identification

Product number -
Other names 2-Chloroethyl 4-fluorophenyl sulphone

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:33330-46-0 SDS

33330-46-0Relevant academic research and scientific papers

One-Step Synthesis of [18F]Fluoro-4-(vinylsulfonyl)benzene: A Thiol Reactive Synthon for Selective Radiofluorination of Peptides

Ma, Gaoyuan,McDaniel, James W.,Murphy, Jennifer M.

supporting information, p. 530 - 534 (2021/01/13)

Radiolabeled peptide-based molecular imaging probes exploit the advantages of large biologics and small molecules, providing both exquisite selectivity and favorable pharmacokinetic properties. Here, we report an operationally simple and broadly applicable approach for the 18F-fluorination of unprotected peptides via a new radiosynthon, [18F]fluoro-4-(vinylsulfonyl)benzene. This reagent demonstrates excellent chemoselectivity at the cysteine residue and rapid 18F-labeling of a diverse scope of peptides to generate stable thioether constructs.

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