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196614

Sigma-Aldrich

2,6-Difluoroaniline

≥97%

Sinonimo/i:

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

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About This Item

Formula condensata:
F2C6H3NH2
Numero CAS:
5509-65-9
Peso molecolare:
129.11
Beilstein:
2802697
Numero CE:
226-853-0
Numero MDL:
MFCD00007655
Codice UNSPSC:
12352100
ID PubChem:
24851775
NACRES:
NA.22

Livello qualitativo

200

Saggio

≥97%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.508 (lit.)

P. eboll.

51-52 °C/15 mmHg (lit.)

Densità

1.199 g/mL at 25 °C (lit.)

Gruppo funzionale

fluoro

Stringa SMILE

Nc1c(F)cccc1F

InChI

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

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Applicazioni

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

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Warning

Indicazioni di pericolo

H226,H302 + H312 + H332,H317

Classi di pericolo

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

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

123.8 °F - closed cup

Punto d’infiammabilità (°C)

51 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBK4647
STBJ6176
STBJ4840
STBJ3648
STBJ2222

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Sigma-Aldrich

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Sigma-Aldrich

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4-Fluoroaniline

2,6-Difluorobenzoic acid 98%

Sigma-Aldrich

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2,6-Difluorobenzoic acid

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Sigma-Aldrich

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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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