196614
2,6-二氟苯胺
≥97%
别名:
2,6-二氟苯胺
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关于此项目
线性分子式:
F2C6H3NH2
化学文摘社编号:
分子量:
129.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-853-0
Beilstein/REAXYS Number:
2802697
MDL number:
Assay:
≥97%
Form:
liquid
Quality Level
assay
≥97%
form
liquid
refractive index
n20/D 1.508 (lit.)
bp
51-52 °C/15 mmHg (lit.)
density
1.199 g/mL at 25 °C (lit.)
functional group
fluoro
SMILES string
Nc1c(F)cccc1F
InChI
1S/C6H5F2N/c7-4-2-1-3-5(8)6(4)9/h1-3H,9H2
InChI key
ODUZJBKKYBQIBX-UHFFFAOYSA-N
Application
2,6-二氟苯胺用于合成：
- 除草化合物N-2,6-二氟苯基-5-甲氧基-1,2,4-三唑并[1,5-a]嘧啶-2-磺酰胺
- p38α激酶的2,6,9-三取代嘌呤抑制剂系列
- 活性药物中间体取代苯基硫代吗啉二氧化物
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Sens. 1
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
123.8 °F - closed cup
flash_point_c
51 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 196614-5G | 04061838762146 |
| 196614-25G | 04061838762139 |
| 196614-100G | 04061838346933 |