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766-49-4

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766-49-4 Usage

Chemical Properties

clear yellow to brownish liquid

Uses

Different sources of media describe the Uses of 766-49-4 differently. You can refer to the following data:
1. Employed in studies on the polymerization1 and cross-coupling2 of phenylacetylenes.
2. 1-Ethynyl-2-fluorobenzene has been employed in the cross-coupling of phenylacetylenes. It may be used in the preparation of 3-(2-deoxy-β-D-ribofuranosyl)-6-(2-fluorophenyl)-2,3-dihydrofuro-[2,3-d]pyrimidin-2-one and 4-(2-fluorophenylethynyl)-3-methyl-5-phenylisoxazole.

Application

1-Ethynyl-2-fluorobenzene has been employed in the cross-coupling of phenylacetylenes. It may be used in the preparation of 3-(2-deoxy-β-D-ribofuranosyl)-6-(2-fluorophenyl)-2,3-dihydrofuro-[2,3-d]pyrimidin-2-one and 4-(2-fluorophenylethynyl)-3-methyl-5-phenylisoxazole.1-Ethynyl-2-fluorobenzene, a fluorinated benzene derivative, is a terminal alkyne.

General Description

1-Ethynyl-2-fluorobenzene, a fluorinated benzene derivative, is a terminal alkyne.

Check Digit Verification of cas no

The CAS Registry Mumber 766-49-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 766-49:
(5*7)+(4*6)+(3*6)+(2*4)+(1*9)=94
94 % 10 = 4
So 766-49-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F/c1-2-7-5-3-4-6-8(7)9/h1,3-6H

766-49-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Price
  • Detail
  • TCI America

  • (E0654)  1-Ethynyl-2-fluorobenzene  >97.0%(GC)

  • 766-49-4

  • 5g

  • 990.00CNY

  • Detail
  • Alfa Aesar

  • (H60596)  2-Fluorophenylacetylene, 97%   

  • 766-49-4

  • 250mg

  • 311.0CNY

  • Detail
  • Alfa Aesar

  • (H60596)  2-Fluorophenylacetylene, 97%   

  • 766-49-4

  • 1g

  • 916.0CNY

  • Detail
  • Aldrich

  • (467006)  1-Ethynyl-2-fluorobenzene  97%

  • 766-49-4

  • 467006-1G

  • 1,633.32CNY

  • Detail

766-49-4SDS

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 1-Ethynyl-2-fluorobenzene

1.2 Other means of identification

Product number -
Other names 1-ETHYNYL-2-FLUOROBENZENE

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:766-49-4 SDS

766-49-4Relevant articles and documents

Synthesis and Photochemical Application of Hydrofluoroolefin (HFO) Based Fluoroalkyl Building Block

Varga, Bálint,Tóth, Balázs L.,Béke, Ferenc,Csenki, János T.,Kotschy, András,Novák, Zoltán

supporting information, p. 4925 - 4929 (2021/07/01)

A novel fluoroalkyl iodide was synthesized on multigram scale from refrigerant gas HFO-1234yf as cheap industrial starting material in a simple, solvent-free, and easily scalable process. We demonstrated its applicability in a metal-free photocatalytic ATRA reaction to synthesize valuable fluoroalkylated vinyl iodides and proved the straightforward transformability of the products in cross-coupling chemistry to obtain conjugated systems.

Visible-Light-Promoted Vinylation of Tetrahydrofuran with Alkynes through Direct C-H Bond Functionalization

Li, Jing,Zhang, Jing,Tan, Haibo,Wang, David Zhigang

supporting information, p. 2522 - 2525 (2015/05/27)

(Chemical Equation Presented) Mild and direct C-H bond functionalizations and vinylations of tetrahydrofuran with alkynes have been accomplished through visible light photocatalysis, yielding a range of vinyl tetrahydrofurans under the synergistic actions of organic dye-type photocatalyst eosin Y, tert-butyl hydroperoxide (t-BuOOH), and a 45 W household lightbulb. A significant kinetic isotope effect (KIE) was recorded, which helps shed light on the mechanistic course.

Process for the preparation of tryptase inhibitors

-

Page/Page column 38, (2008/06/13)

This invention is directed to processes for the preparation of compounds of the formula I and their salts, which are useful as tryptase inhibitors, to intermediates useful in the preparation of such compounds, to processes for the preparation of such inte

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