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196614

Sigma-Aldrich

2,6-Difluoroaniline

≥97%

Sinônimo(s):

2,6-Difluorobenzenamine, 2,6-Difluorobenzeneamine, 2,6-Difluorophenylamine

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About This Item

Fórmula linear:
F2C6H3NH2
Número CAS:
5509-65-9
Peso molecular:
129.11
Beilstein:
2802697
Número CE:
226-853-0
Número MDL:
MFCD00007655
Código UNSPSC:
12352100
ID de substância PubChem:
24851775
NACRES:
NA.22

Ensaio

≥97%

forma

liquid

índice de refração

n20/D 1.508 (lit.)

pb

51-52 °C/15 mmHg (lit.)

densidade

1.199 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

Nc1c(F)cccc1F

InChI

1S/C6H5F2N/c7-4-2-1-3-5(8)6(4)9/h1-3H,9H2

chave InChI

ODUZJBKKYBQIBX-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Aplicação

2,6-Difluoroaniline was used in the synthesis of:
  • N-2,6-difluorophenyl-5-methoxy-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide, herbicidal compound
  • series of 2,6,9-trisubstituted purine inhibitors of p38α kinase
  • substituted phenylthiomorpholine dioxide, an active pharmaceutical intermediate

Pictogramas

FlameExclamation mark
GHS02,GHS07

Palavra indicadora

Warning

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Sens. 1

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

123.8 °F - closed cup

Ponto de fulgor (°C)

51 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Sigma-Aldrich

186783

2,6-Difluorobenzonitrile

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Sigma-Aldrich

F3800

4-Fluoroaniline

2,6-Difluorobenzoic acid 98%

Sigma-Aldrich

190039

2,6-Difluorobenzoic acid

1-Bromo-2,6-difluorobenzene 98%

Sigma-Aldrich

263451

1-Bromo-2,6-difluorobenzene

Zehong Wan et al.
Bioorganic & medicinal chemistry letters, 13(6), 1191-1194 (2003-03-20)
The design, synthesis and SAR of a series of 2,6,9-trisubstituted purine inhibitors of p38alpha kinase is reported. Synthetic routes were devised to allow for array synthesis in which all three points of diversity could be facilely explored. The binding of
Chao-Nan Chen et al.
Bioorganic & medicinal chemistry, 17(8), 3011-3017 (2009-04-04)
Triazolopyrimidine-2-sulfonamide belongs to a herbicide group called acetohydroxyacid synthase inhibitors. With the aim to discover new triazolopyrimidine sulfonanilide compounds with high herbicidal activity and faster degradation rate in soil, the methyl group of Flumetsulam (FS) was modified into a methoxy
Catalyzed double Michael addition of anilines to vinyl sulfone.
Chen JJ, et al.
Tetrahedron Letters, 44(17), 3459-3462 (2003)
Irudayaraj Bernadette Amali et al.
Applied biochemistry and biotechnology, 190(2), 373-390 (2019-08-01)
In this article, we have reported the preparation and structural characterization of a new Schiff base ligand (E)-2-(((2,6-difluorophenyl)imino)methyl)phenol (HSBL) and its derived metal(II) complexes [Cu(SBL)2] (1), [Ni(SBL)2] (2) and [Pd(SBL)2] (3). Using various analytical and spectroscopic techniques, their structural properties
Simone K Schmidt et al.
Chirality, 29(1), 48-56 (2016-12-27)
For the enantiopure synthesis of novel chiral GABA uptake inhibitors, nipecotic acid (1) is an important key precursor. To characterize accurately the pharmacological activity of these interesting target compounds, the determination of the correct enantiomeric purity of nipecotic acid as
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