1513-65-1

  • Product Name:2,6-Difluoropyridine
  • Molecular Formula:C5H3F2N
  • Purity:99%
  • Molecular Weight:115.082
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Product Details

Manufacturers supply cost-effective and customizable 2,6-Difluoropyridine 1513-65-1

  • Molecular Formula:C5H3F2N
  • Molecular Weight:115.082
  • Appearance/Colour:Colorless to light yellow liquid 
  • Vapor Pressure:0.643mmHg at 25°C 
  • Refractive Index:n20/D 1.437(lit.)  
  • Boiling Point:134.3 °C at 760 mmHg 
  • PKA:-6.09±0.10(Predicted) 
  • Flash Point:33.9 °C 
  • PSA:12.89000 
  • Density:1.263 g/cm3 
  • LogP:1.35980 

2,6-Difluoropyridine(Cas 1513-65-1) Usage

General Description

Lithium diisopropylamide (LDA)-mediated ortholithiations of 2,6-difluoropyridine in tetrahydrofuran at -78°C has been studied using a combination of IR and NMR spectroscopic and computational methods. Polycondensation of bistrimethylsilyl derivatives of various diphenols with 2,6-difluoropyridine in N-methylpyrrolidone in the presence of K2CO3 has been investigated.

InChI:InChI=1/C5H4F3N3O/c6-5(7,8)2-1-3(12)11-4(9)10-2/h1H,(H3,9,10,11,12)

1513-65-1 Relevant articles

Highly reactive and regenerable fluorinating agent for oxidative fluorination of aromatics

Janmanchi, Krishna Murthy,Dolbier Jr., William R.

, p. 349 - 354 (2008)

A newly synthesized copper aluminum fluo...

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Boudakian, Max M.

, p. 497 - 506 (1981)

The isolation and stabilization of elusi...

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Lui et al.

, p. 583 (1978)

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Method for efficiently synthesizing fluorine-containing compound

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Paragraph 0074-0076, (2021/06/26)

The invention discloses a method for eff...

PROCESS FOR FLUORINATING COMPOUNDS

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Page/Page column 29; 33; 35, (2017/02/28)

Disclosed are mild temperature (e.g., fr...

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[CpRhCl(μ-Cl)]2 is reported as a highly ...

Acyl azolium fluorides for room temperature nucleophilic aromatic fluorination of chloro- and nitroarenes

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The reaction of acid fluorides with N-he...

1513-65-1 Process route

pyridine
110-86-1

pyridine

2,6-difluoro pyridine
1513-65-1

2,6-difluoro pyridine

2-fluoropyridine
372-48-5

2-fluoropyridine

Conditions
Conditions Yield
With co-precipitated copper aluminum fluoride (CuAl01); at 500 ℃; Gas phase; Inert atmosphere;
32%
11%
With Al2CuF8; at 500 ℃; Reagent/catalyst; Inert atmosphere;
32%
11%
With iodine; fluorine; In 1,1,2-Trichloro-1,2,2-trifluoroethane; at 0 ℃; Yield given; Yields of byproduct given;
With iodine; fluorine; In 1,1,2-Trichloro-1,2,2-trifluoroethane; at 0 ℃; Yields of byproduct given;
3 % Chromat.
pyridine
110-86-1

pyridine

perfluoro-N-ethylpyrrolidine
2344-10-7

perfluoro-N-ethylpyrrolidine

2,6-difluoro pyridine
1513-65-1

2,6-difluoro pyridine

Pentafluoropyridine
700-16-3

Pentafluoropyridine

N,N-Bis(trifluoromethyl)amine
371-77-7

N,N-Bis(trifluoromethyl)amine

Conditions
Conditions Yield
With caesium tetrafluorocobaltate(III); In gaseous matrix; at 310 ℃; for 3.5h; Further byproducts given;
35.3%
13.6%
8.2%
1.6%

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