D102504
1,5-二氟-2,4-二硝基苯
97%
别名:
DFDNB
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关于此项目
线性分子式:
F2C6H2(NO2)2
化学文摘社编号:
分子量:
204.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-324-0
Beilstein/REAXYS Number:
1883116
MDL number:
Assay:
97%
Form:
powder
InChI
1S/C6H2F2N2O4/c7-3-1-4(8)6(10(13)14)2-5(3)9(11)12/h1-2H
InChI key
VILFTWLXLYIEMV-UHFFFAOYSA-N
SMILES string
[O-][N+](=O)c1cc(c(F)cc1F)[N+]([O-])=O
assay
97%
form
powder
mp
72-74 °C (lit.)
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - STOT RE 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Suman Thummanagoti et al.
Molecular diversity, 15(1), 101-107 (2010-03-20)
Traceless synthesis of 2-aminoimidazoquinoxalinones has been performed on soluble polymer support under open-vessel microwave dielectric heating. The reaction progression is monitored directly by the conventional proton NMR which indicated no release of the substrate from the support. Fmoc-deprotected amino acid
Gang Liu et al.
Journal of combinatorial chemistry, 9(1), 70-78 (2007-01-09)
This paper describes our recent efforts to synthesize novel compound scaffolds integrating 2-quinoxalinol with privileged structures of 1,3-dihydro-benzoimidazol-2-one, 1,3-dihydro-benzoimidazole-2-thione, 3-hydroxy-1H-quinoxalin-2-one, 2H-benzo[1,4]oxazin-3-ol, 2H-benzo[1,4]thiazin-3-ol, and 1,3,4,5-tetrahydro-benzo[1,4]diazepin-2-one, respectively. Eight novel benzofused tricycles and their substituent diversity points were developed. These include pyrazino[2,3-g]quinoxaline-2,8-diol (I)
S M Hourani et al.
General pharmacology, 20(4), 413-416 (1989-01-01)
1. The effects of some possible inhibitors of ectonucleotidases on the breakdown of extracellular ATP by strips of guinea-pig urinary bladder were investigated. 2. Suramin and ethacrynic acid (10 mM) both inhibited ATP breakdown significantly, and difluorodinitrobenzene (10 mM) inhibited
Dong Mei Wang et al.
Journal of combinatorial chemistry, 11(4), 556-575 (2009-05-28)
This paper reports a versatile, good-yielding, solution-phase method that is a substituent diversity-directed synthesis of 1H-indoles (6-13, 17-20) and 1-hydroxyindoles (14, 15) starting from commercially available 1,5-difluoro-2,4-dinitrobenzene. The synthetic products possessed the maximum six diversity points.
S Simonsson et al.
The Journal of biological chemistry, 273(38), 24633-24639 (1998-09-12)
The UL9 gene of herpes simplex virus type 1 (HSV-1) encodes an origin binding protein (OBP). It is an ATP-dependent DNA helicase and a sequence-specific DNA-binding protein. The latter function is carried out by the C-terminal domain of OBP (DeltaOBP).
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