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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
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Sens. 1
保管分類コード
3 - Flammable liquids
WGK
WGK 3
引火点(°F)
123.8 °F - closed cup
引火点(℃)
51 °C - closed cup
個人用保護具 (PPE)
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
消防法
第4類:引火性液体
第二石油類
危険等級III
非水溶性液体
Jan Code
196614-5G:
196614-100G:
196614-VAR:
196614-25G:
196614-BULK:
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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
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)
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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