N109
1-萘甲醛
95%
别名:
α-萘亚甲基, 萘-1-甲醛, α-萘甲醛
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线性分子式:
C10H7CHO
化学文摘社编号:
分子量:
156.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-633-4
Beilstein/REAXYS Number:
386082
MDL number:
Assay:
95%
Form:
liquid
InChI
1S/C11H8O/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-8H
InChI key
SQAINHDHICKHLX-UHFFFAOYSA-N
SMILES string
[H]C(=O)c1cccc2ccccc12
vapor density
>1 (vs air)
assay
95%
form
liquid
refractive index
n20/D 1.652 (lit.)
bp
160-161 °C/15 mmHg (lit.)
mp
1-2 °C (lit.)
density
1.15 g/mL at 25 °C (lit.)
Quality Level
Application
1-萘甲醛可用于合成：
- ( S )-1-α-萘基-1-乙醇
- N -（4-芳基）- N -（α-萘基）胺
- N -芳基- N - [1-（1-萘基）丁-3-烯基]
- 胺萘-1-羧酸甲酯
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Pramod Kumar Singh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 64(4), 853-858 (2006-03-15)
A series of new coordination complexes of cobalt(II), nickel(II) and copper(II) with two new aroylhydrazones, 2-hydroxy-1-naphthaldehyde isonicotinoylhydrazone (H(2)L(1)) and 2-hydroxy-1-naphthaldehyde-2-thenoyl-hydrazone (H(2)L(2)) have been synthesized and characterized by elemental analysis, conductance measurements, magnetic susceptibility measurements, (1)H NMR spectroscopy, IR spectroscopy, electronic
Cytotoxic and Antifungal Activities of Diverse ?-Naphthylamine Derivatives.
Kouznetsov V, et al.
Scientia Pharmaceutica, 80(4), 867-878 (2012)
Highly enantioselective addition of dimethylzinc to arylaldehydes catalyzed by (2S)-1-ferrocenyl-methylaziridin-2-yl (diphenyl) methanol.
Wang M, et al.
Tetrahedron Asymmetry, 20(3), 288-292 (2009)
Miraç Ocak et al.
Journal of fluorescence, 27(1), 59-68 (2016-09-17)
Four new Schiff base ligands carrying naphthalene groups were prepared from the reaction of 2,4-diamino-6-methyl-1,3,5-triazine and 2,4-diamino-6-undecyl-1,3,5-triazine with 2-hydroxy-1-naphthaldehyde. The influence of a series of metal ions including Cu
Transformation of schiff bases derived from alpha?naphthaldehyde. Synthesis, spectral data and biological activity of new?3?aryl?2?(??naphtyl)?4?thiazolidinones and N?aryl?N?[1?(??naphthyl) but?3?enyl] amines.
Kouznetsov V, et al.
Journal of Heterocyclic Chemistry, 41(6), 995-999 (2004)
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