70190
2-Naphthaldehyde
purum, ≥95.0% (GC)
Synonym(s):
β-Naphthaldehyde
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About This Item
Linear Formula:
C10H7CHO
CAS Number:
Molecular Weight:
156.18
EC Number:
200-640-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
507750
MDL number:
grade
purum
assay
≥95.0% (GC)
impurities
≤1% free acid
mp
58-61 °C
SMILES string
[H]C(=O)c1ccc2ccccc2c1
InChI
1S/C11H8O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-8H
InChI key
PJKVFARRVXDXAD-UHFFFAOYSA-N
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Kyung-Don Kang et al.
Analytical biochemistry, 344(2), 183-192 (2005-08-09)
We have previously reported the synthesis of four alpha-cyano-containing ethers based on 2-naphthaldehyde (2-NA) as cytochrome P450 (P450) fluorescent substrates. Activity detection was based on the formation of fluorescent 2-NA following substrate hydrolysis. A major limitation of these substrates was
Takayoshi Awakawa et al.
Bioorganic & medicinal chemistry letters, 22(13), 4338-4340 (2012-05-29)
Bostrycoidin and fusarubin are biologically active fungal polyketides produced by Nectria haematococca. This azaanthraquinone and naphthoquinone are thought to be biosynthesized via formation of a C(14) heptaketide aldehyde as a common key intermediate. A BLAST search against the genome of
Fernanda Spezia Pedrini et al.
The Journal of pharmacy and pharmacology, 62(9), 1128-1136 (2010-08-28)
New compounds with biological targets and less cytotoxicity to normal cells are necessary for cancer therapy. In this work ten synthetic chalcones derived from 2-naphtaldehyde were evaluated for their cytotoxic effect in murine acute lymphoblastic leukemia cells L-1210. A series