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Key Documents

454281

Sigma-Aldrich

2-Fluoro-5-nitrobenzaldehyde

97%

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About This Item

Linear Formula:
FC6H3(NO2)CHO
CAS Number:
Molecular Weight:
169.11
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

57-60 °C (lit.)

functional group

aldehyde
fluoro
nitro

SMILES string

[O-][N+](=O)c1ccc(F)c(C=O)c1

InChI

1S/C7H4FNO3/c8-7-2-1-6(9(11)12)3-5(7)4-10/h1-4H

InChI key

VVXFDFQEIRGULC-UHFFFAOYSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Facile solid phase synthesis of 1, 2-disubstituted-6-nitro-1, 4-dihydroquinazolines using a tetrafunctional scaffold.
Wang X MLA, et al.
Tetrahedron Letters, 46(3), 427-430 (2005)
J Craig Ruble et al.
Journal of the American Chemical Society, 131(11), 3991-3997 (2009-03-06)
PNU-286607 is the first member of a promising, novel class of antibacterial agents that act by inhibiting bacterial DNA gyrase, a target of clinical significance. Importantly, PNU-286607 displays little cross-resistance with marketed antibacterial agents and is active against methicillin-resistant staphylococcus
Novel synthesis of dibenzo [b,g] 1, 5-oxazocines.
Ouyang X and Kiselyov AS.
Tetrahedron Letters, 40(32), 5827-5830 (1999)
The preparation of some polymethine astrazon dyes.
Gale DJ and Wilshire JFK.
Australian Journal of Chemistry, 23(5), 1063-1068 (1970)
A valuable heterocyclic ring transformation: from isoxazolin-5 (2H)-ones to quinolines.
Abbiati G, et al.
Tetrahedron, 59(50), 9887-9893 (2003)

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