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D102504

Sigma-Aldrich

1,5-Difluoro-2,4-dinitrobenzene

97%

Sinónimos:

DFDNB

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About This Item

Fórmula lineal:
F2C6H2(NO2)2
Número de CAS:
327-92-4
Peso molecular:
204.09
Beilstein/REAXYS Number:
1883116
EC Number:
206-324-0
MDL number:
MFCD00007052
UNSPSC Code:
12352100
PubChem Substance ID:
24893327
NACRES:
NA.22

assay

97%

form

powder

mp

72-74 °C (lit.)

SMILES string

[O-][N+](=O)c1cc(c(F)cc1F)[N+]([O-])=O

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

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pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - STOT RE 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
BCCG3173
BCCC6132
BCCB3687
BCBX1748
BCBW9106

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1,4-Dinitrobenzene 98%

Sigma-Aldrich

102369

1,4-Dinitrobenzene

Piperidine ReagentPlus®, 99%

Sigma-Aldrich

104094

Piperidine

Zhanguo Wang et al.
Journal of combinatorial chemistry, 9(4), 652-660 (2007-05-17)
This paper discusses the synthesis of privileged structures 4H-benzo[1,4]thiazin-3-one and 1,1-dioxo-1,4-dihydro-2H-1lambda6-benzo[1,4]thiazin-3-one derivatives in a parallel solution-phase manner using 1,5-difluoro-2,4-dinitrobenzene. Each scaffold possesses four diversity points. A cheap and efficient oxidant, urea-hydrogen peroxide (UHP), was applied for the introduction of the
Yunyun Yuan et al.
Journal of combinatorial chemistry, 9(1), 158-170 (2007-01-09)
This paper discusses the synthesis of benzo[1,4]oxazin-3-one-based compounds from 1,5-difluoro-2,4-dinitrobenzene (1), including benzo[1,4]oxazin-3-ones (5-11) and five novel benzo[1,4]oxazin-3-one-based tricycles: 6-hydroxy-4H-1-oxa-4,5,8-triazaanthracen-3-one (14), 3,8-dihydro-5-oxa-1,3,8-triazacyclopenta-[b]-naphthalene-7-one (15, 17, 21), 3,8-dihydro-5-oxa-1,2,3,8-tetraazacylopenta[b]-naphthalene-7-one (16, 20), 3,8-dihydro-1H-5-oxa-1,3,8-triazacyclopenta[b]-naphthalene-2,7-dione (18, 22), and 5,8-dihydro-4H-1-oxa-4,5,8-triazaanthracene-3,6,7-trione (19). Finally, a chemical library based on
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).
Yanshun Liu et al.
Protein science : a publication of the Protein Society, 11(2), 371-380 (2002-01-16)
When concentrated in mildly acidic solutions, bovine pancreatic ribonuclease (RNase A) forms long-lived oligomers including two types of dimer, two types of trimer, and higher oligomers. In previous crystallographic work, we found that the major dimeric component forms by a
Alexander Shivanyuk et al.
Organic letters, 4(9), 1555-1558 (2002-04-27)
[reaction: see text]. o-alkylation of C2V-symmetrical resorcinarene tetraesters 2 with 2 equiv of 1,3-difluoro-4,6-dinitrobenzene readily affords conformationally rigid octanitro resorcinarene 3, which is a potential scaffold for the design of supramolecular structures.
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