
CAS 66-99-9: 2-Naphthalenecarboxaldehyde
Formula:C11H8O
InChI:InChI=1S/C11H8O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-8H
InChI key:InChIKey=PJKVFARRVXDXAD-UHFFFAOYSA-N
SMILES:C(=O)C1=CC2=C(C=C1)C=CC=C2
Synonyms:- 2-Formylanaphthalene
- 2-Formylnaphthalene
- 2-Naftaldehido
- 2-Naphtaldehyde
- 2-Naphthakdehyde
- 2-Naphthaldehyd
- 2-Naphthaldehyde (Beta)
- 2-Naphthalenealdehyde
- 2-Naphthalenecarboxaldehyde
- 2-Naphthylaldehyde
- 2-Naphthylcarboxaldehyde
- See more synonyms
Sort by
Found 8 products.
2-Naphthaldehyde
CAS:Formula:C11H8OPurity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:156.182-Naphthaldehyde, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C11H8OPurity:98%Color and Shape:Off-white to yellow to light beige, Powder and/or chunksMolecular weight:156.182-Naphthaldehyde
CAS:Purity:95.00%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:156.18400573730472-Naphthaldehyde, 98%
CAS:2-Naphthaldehyde aids in stereo-selective formation of bicyclo 2-siloxy-2-alkoxyoxetanes. It is also used as catalytic agent and petrochemical additive. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C11H8OPurity:98%Color and Shape:White to cream, Crystals or powder or crystalline powder or lumpsMolecular weight:156.182-Naphthaldehyde
CAS:2-Naphthaldehyde is an antimicrobial agent that has been shown to inhibit the growth of bacteria in vitro. It has been shown to inhibit the synthesis of DNA, RNA and protein. 2-Naphthaldehyde is an intramolecular hydrogen acceptor and a substrate for coumarin derivatives. The reaction mechanism of 2-napthalaldehyde is not yet fully understood, but it has been proposed that 2-napthalaldehyde reacts with sodium carbonate to form sodium phenolate and acetone. 2-Naphthaldehyde also shows genotoxic activity, as it has been shown to induce structural aberrations in bacterial DNA. This chemical compound also forms coordination geometry complexes with metal ions such as copper and zinc.Formula:C11H8OPurity:Min. 98%Color and Shape:Beige PowderMolecular weight:156.18 g/mol2-Naphthaldehyde
CAS:2-NaphthaldehydeFormula:C11H8OPurity:98%Color and Shape: white solidMolecular weight:156.18g/mol