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Quinoxaline, 2-fluoro- (7CI,8CI,9CI) is a chemical compound belonging to the quinoxaline family, characterized by the presence of a fluorine atom at the 2-position. It is an organic heterocyclic compound with the molecular formula C8H5N2F and a molecular weight of 144.14 g/mol. Quinoxaline, 2-fluoro- (7CI,8CI,9CI) is primarily used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. The presence of the fluorine atom in the molecule can significantly influence its physical, chemical, and biological properties, making it an important intermediate in the development of new compounds with potential applications in various industries.

2712-12-1

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2712-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2712-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2712-12:
(6*2)+(5*7)+(4*1)+(3*2)+(2*1)+(1*2)=61
61 % 10 = 1
So 2712-12-1 is a valid CAS Registry Number.

2712-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoroquinoxaline

1.2 Other means of identification

Product number -
Other names 2-Fluor-chinoxalin

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:2712-12-1 SDS

2712-12-1Downstream Products

2712-12-1Relevant academic research and scientific papers

Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides

Arisawa, Mieko,Tanii, Saori,Tazawa, Takeru,Yamaguchi, Masahiko

supporting information, p. 11390 - 11393 (2016/09/23)

A rhodium complex catalyzed the conversion of the C-O bond of heteroaryl aryl ethers to the C-F bond. The reaction of (4-chlorophenylthio)pentafluorobenzene with heteroaryl aryl ethers provided heteroaryl fluorides and heteroaryl (4-chlorophenylthio)tetrafluorophenyl ethers; this involved the cleavage of a single heteroaryl C-O bond under equilibrium conditions. The reaction of heteroaryl aryl ethers with 2-fluorobenzothiazole in which two heteroaryl and aryl C-O bonds were cleaved provided heteroaryl fluorides and aryl fluorides. The reactions were applicable to five-membered and six-membered heteroaryl aryl ethers and also to diaryl ethers possessing one or two electron-withdrawing groups.

Elemental fluorine. Part 10.1 Selective fluorination of pyridine, quinoline and quinoxaline derivatives with fluorine-iodine mixtures

Chambers, Richard D.,Parsons, Mandy,Sandford, Graham,Skinner, Christopher J.,Atherton, Malcolm J.,Moilliet, John S.

, p. 803 - 810 (2007/10/03)

Selective fluorination of a range of pyridine and quinoline substrates to give corresponding 2-fluoro-derivatives can be readily achieved in high yield at room temperature using elemental fluorine-iodine mixtures. Reaction of fluorine with iodine forms, in situ, systems that function like sources of both iodonium and fluoride ions and fluorination of heterocyclic derivatives is suggested to proceed by fluoride ion attack on intermediate W-iodo-heterocyclic species. Quinoxaline derivatives react under similar conditions to give either the 2-fluoro- or 2,3-difluoro-quinoxaline derivatives depending on the ratio of fluorine passed through the solution. In related processes, pyridine can be alkoxylated upon reaction of an appropriate alcohol and fluorine.

Process for the preparation of fluorinated heterocyclic compounds

-

, (2008/06/13)

A method of fluorinating a heterocyclic organic compound comprises the step of reacting a heterocyclic compound with elemental fluorine in the presence of another halogen. The reaction may be conducted in the presence of a base.

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