Skip to Content
Merck
All Photos(1)

Key Documents

526819

Sigma-Aldrich

3-Fluoro-4-hydroxy-5-methoxybenzaldehyde

97%

Sign Into View Organizational & Contract Pricing


About This Item

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

Pricing and availability is not currently available.

Quality Level

Assay

97%

mp

114-118 °C (lit.)

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[1] and 4-[(4-hydroxy-3-fluoro-5-methoxy-benzylidene)amino]-1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one.[2]

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

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service