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Details

Stereochemistry ACHIRAL
Molecular Formula C6H2F2N2O4
Molecular Weight 204.0879
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,5-DIFLUORO-2,4-DINITROBENZENE

SMILES

[O-][N+](=O)C1=CC(=C(F)C=C1F)[N+]([O-])=O

InChI

InChIKey=VILFTWLXLYIEMV-UHFFFAOYSA-N
InChI=1S/C6H2F2N2O4/c7-3-1-4(8)6(10(13)14)2-5(3)9(11)12/h1-2H

HIDE SMILES / InChI

Molecular Formula C6H2F2N2O4
Molecular Weight 204.0879
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Unprecedented tunable tetraazamacrocycles.
2010-06-18
IL-13 from Th2-type cells suppresses induction of antigen-specific Th1 immunity in a T-cell lymphoma.
2010-01
Reversed-phase high-performance liquid chromatographic enantioresolution of six beta-blockers using dinitrophenyl-L-Pro-N-hydroxysuccinimide ester, N-succinimidyl-(S)-2-(6-methoxynaphth-2-yl) propionate and twelve variants of Sanger's reagent as chiral derivatizing reagents.
2009-12
Substituent diversity-directed synthesis of indole derivatives.
2009-05-28
The glucocorticoid-induced TNF receptor-related protein (GITR)-GITR ligand pathway acts as a mediator of cutaneous dendritic cell migration and promotes T cell-mediated acquired immunity.
2009-03-01
A large population of diverse neurons in the Drosophila central nervous system expresses short neuropeptide F, suggesting multiple distributed peptide functions.
2008-09-19
Synthesis of chiral hydrazine reagents and their application for liquid chromatographic separation of carbonyl compounds via diastereomer formation.
2008-05-09
N-(n-Dec-yl)-4-nitro-aniline.
2008-02-06
Design and synthesis of novel tricycles based on 4H-benzo[1,4]thiazin-3-one and 1,1-dioxo-1,4-dihydro-2H-1lambda6-benzo[1,4]thiazin-3-one.
2007-10-20
Solution-phase parallel synthesis of diverse 1,5-benzodiazepin-2-ones.
2007-10-09
Solution-phase parallel synthesis of 2,3-dihydro-1,5-benzothiazepin-4(5H)-ones.
2007-08-10
Parallel solution-phase synthesis of 4H-benzo[1,4]thiazin-3-one and 1,1-dioxo-1,4-dihydro-2H-1lambda6-benzo[1,4]thiazin-3-one derivatives from 1,5-difluoro-2,4-dinitrobenzene.
2007-05-17
An efficient method for solution-phase parallel synthesis of 2-quinoxalinol salen Schiff-base ligands.
2007-05-15
Triptycene-based expanded oxacalixarenes: synthesis, structure, and tubular assemblies in the solid state.
2007-05-11
Synthesis of diverse benzo[1,4]oxazin-3-one-based compounds using 1,5-difluoro-2,4-dinitrobenzene.
2007-01-09
Solution-phase parallel synthesis of 3,5,6-substituted indolin-2-ones.
2007-01-09
Benzofused tricycles based on 2-quinoxalinol.
2007-01-09
Solution-phase parallel synthesis of a 1,2,7-trialkyl-1H-imidazo[4,5-g]quinoxalin-6-ol library scaffold.
2005-09-13
Synthesis of a phenyl thio-beta-D-galactopyranoside library from 1,5-difluoro-2,4-dinitrobenzene: discovery of efficient and selective monosaccharide inhibitors of galectin-7.
2005-05-21
Synthesis of functionalized oxacalix[4]arenes.
2005-01-06
Multistep parallel synthesis of substituted 5-aminobenzimidazoles in solution phase.
2004-09-14
Oligomerization of ribonuclease A: two novel three-dimensional domain-swapped tetramers.
2004-08-27
Rigid tetranitroresorcinarenes.
2002-05-02
Structures of the two 3D domain-swapped RNase A trimers.
2002-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:54:05 GMT 2025
Edited
by admin
on Mon Mar 31 19:54:05 GMT 2025
Record UNII
G5VV4MQ22V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,5-DIFLUORO-2,4-DINITROBENZENE
Systematic Name English
NSC-10246
Preferred Name English
Code System Code Type Description
FDA UNII
G5VV4MQ22V
Created by admin on Mon Mar 31 19:54:05 GMT 2025 , Edited by admin on Mon Mar 31 19:54:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID6059813
Created by admin on Mon Mar 31 19:54:05 GMT 2025 , Edited by admin on Mon Mar 31 19:54:05 GMT 2025
PRIMARY
PUBCHEM
67598
Created by admin on Mon Mar 31 19:54:05 GMT 2025 , Edited by admin on Mon Mar 31 19:54:05 GMT 2025
PRIMARY
MESH
C002041
Created by admin on Mon Mar 31 19:54:05 GMT 2025 , Edited by admin on Mon Mar 31 19:54:05 GMT 2025
PRIMARY
CAS
327-92-4
Created by admin on Mon Mar 31 19:54:05 GMT 2025 , Edited by admin on Mon Mar 31 19:54:05 GMT 2025
PRIMARY
NSC
10246
Created by admin on Mon Mar 31 19:54:05 GMT 2025 , Edited by admin on Mon Mar 31 19:54:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-324-0
Created by admin on Mon Mar 31 19:54:05 GMT 2025 , Edited by admin on Mon Mar 31 19:54:05 GMT 2025
PRIMARY