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278688 Sigma-Aldrich

9-Anthracenecarboxaldehyde

97%

Synonym: 9-Anthraldehyde

  • CAS Number 642-31-9

  • Empirical Formula (Hill Notation) C15H10O

  • Molecular Weight 206.24

  •  Beilstein/REAXYS Number 639167

  •  EC Number 211-383-0

  •  MDL number MFCD00001254

  •  PubChem Substance ID 24856824

  •  NACRES NA.22

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Properties

Related Categories Aldehydes, Biochemicals and Reagents, Building Blocks, C13-C60, Carbonyl Compounds,
assay   97%
mp   103-105 °C (lit.)
SMILES string   [H]C(=O)c1c2ccccc2cc3ccccc13
InChI   1S/C15H10O/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-10H
InChI key   YMNKUHIVVMFOFO-UHFFFAOYSA-N

Description

General description

The Diels-Alder reaction of 9-anthracenecarboxaldehyde with benzenediazonium-2-carboxylate was studied.

Application

9-Anthracenecarboxaldehyde has been used in the synthesis of:
• new asymmetrical tridentate Schiff base ligands
• 2-(9-anthrylmethyl-ideneamino)-4-methyl-phenol, novel Schiff base via condensation with 2-amino-p-cresol
• functionalized ligand, 2-(anthracen-9-ylidene)-4,5-bis(diphenylphosphino)-4-cyclopentene-1,3-dione via Knoevenangel condensation with the diphosphine ligand 4,5-bis(diphenylphosphino)-4-cyclopentene-1,3-dione

Packaging

5, 25, 100 g in glass bottle

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable
Protocols & Articles

Articles

Sensor Dyes

In 1998 R.F. Furchgott, L.J. Ignarro, and F. Murad received the Nobel Prize in Physiology and Medicine for their discoveries concerning nitric oxide as a signaling molecule in the cardiovascular syst...
Monika Baeumle
BioFiles 2011, 6.3, 23.
Keywords: Applications, Biochemistry, Biological processes, Cancer, Cardiovascular, Central Nervous System, Diseases, Extinction coefficient, Indicators, Inflammation, Methods, Microscopy, Neurotransmission, Sol-gel, Type

Peer-Reviewed Papers
15

References

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