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526819

Sigma-Aldrich

3-Fluoro-4-hydroxy-5-methoxybenzaldehyde

97%

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About This Item

Linear Formula:
FC6H2(OH)(OCH3)CHO
CAS Number:
79418-78-3
Molecular Weight:
170.14
MDL number:
MFCD02683560
UNSPSC Code:
12352100
PubChem Substance ID:
24874580
NACRES:
NA.22

Quality Level

100

assay

97%

mp

114-118 °C (lit.)

functional group

aldehyde
fluoro

SMILES string

COc1cc(C=O)cc(F)c1O

InChI

1S/C8H7FO3/c1-12-7-3-5(4-10)2-6(9)8(7)11/h2-4,11H,1H3

InChI key

OOGOFUKAJDPHDJ-UHFFFAOYSA-N

General description

3-Fluoro-4-hydroxy-5-methoxybenzaldehyde is an aryl fluorinated building block.

Application

3-Fluoro-4-hydroxy-5-methoxybenzaldehyde may be used to synthesize 3-(3-fluoro-4-hydroxy-5-methoxyphenyl)-N-phenethylacrylamide and 4-[(4-hydroxy-3-fluoro-5-methoxy-benzylidene)amino]-1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBR9838V
MKBQ1517V
00727DH
09303AH
10408LE

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The new Schiff base 4-[(4-Hydroxy-3-fluoro-5-methoxy-benzylidene) amino]-1, 5-dimethyl-2-phenyl-1, 2-dihydro-pyrazol-3-one: Experimental, DFT calculational studies and in vitro antimicrobial activity.
Iskeleli NO, et al.
Spectrochimica Acta Part A: Molecular Spectroscopy, 139, 356-366 (2015)
John Yang et al.
Bioorganic & medicinal chemistry, 18(14), 5032-5038 (2010-07-06)
A series of catechol ring-fluorinated derivatives of caffeic acid phenethyl amide (CAPA) were synthesized and screened for cytoprotective activity against H2O2 induced oxidative stress in human umbilical vein endothelial cells (HUVEC). CAPA and three fluorinated analogs were found to be

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