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518301

Sigma-Aldrich

4-Fluoro-3-nitrobenzaldehyde

97%

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About This Item

Linear Formula:
FC6H3(NO2)CHO
CAS Number:
42564-51-2
Molecular Weight:
169.11
MDL number:
MFCD01861388
UNSPSC Code:
12352100
PubChem Substance ID:
24874009
NACRES:
NA.22

Assay

97%

mp

45-47 °C (lit.)

SMILES string

[O-][N+](=O)c1cc(C=O)ccc1F

InChI

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

InChI key

ILKWFRCNNILIJW-UHFFFAOYSA-N

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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K L Kirk et al.
Journal of medicinal chemistry, 29(10), 1982-1988 (1986-10-01)
2-Fluoro-, 4-fluoro-, and 6-fluorophenylephrine (6-FPE) were synthesized from the corresponding fluorinated 3-hydroxybenzaldehydes. New routes to 2-fluoro- and 6-fluoro-3-hydroxybenzaldehydes were developed based on regioselective lithiation of 2- and 4-[(dimethyl-tert-butylsilyl)oxy]fluorobenzene ortho to fluorine. As with norepinephrine and isoproterenol analogues, the adrenergic properties
C A Hutton
Organic letters, 1(2), 295-297 (2000-05-24)
[formula: see text] Numerous biologically active cyclic peptides, such as the antibiotic vancomycin, contain amino acid residues connected through side-chain biaryl or aryl-alkyl ether linkages. Nucleophilic aromatic substitution reactions have recently been shown to provide a general method for the
Solid phase synthesis of vancomycin mimics.
Arnusch CJ and Pieters RJ.
European Journal of Organic Chemistry, 2003(16), 3131-3138 (2003)
S Chowdhury et al.
The Journal of organic chemistry, 66(19), 6257-6262 (2001-09-18)
With the use of S(N)Ar or Ullmann reactions, the synthesis of the first lower-rim aryl ether derivatives of tert-butylcalix[4]arene is reported, as are some of their conformational properties, (1)H NMR spectra, and X-ray crystal structures. The lower-rim aryl pendants reported

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