N206
2-Naphthaldehyde
98%
Synonym(s):
β-Naphthaldehyde
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About This Item
Linear Formula:
C10H7CHO
CAS Number:
Molecular Weight:
156.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-640-2
Beilstein/REAXYS Number:
507750
MDL number:
Assay:
98%
Form:
crystals
Quality Level
assay
98%
form
crystals
mp
58-61 °C (lit.)
storage temp.
−20°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
Application
2-Naphthaldehyde can be used as a reactant:
- In proline catalyzed aldol reaction.
- In asymmetric three-component Mannich reaction.
- For the synthesis of Hantzsch 1,4-dihydropyridines.13}
- Asymmetric benzoin condensation reaction.
- For the synthesis of pyrazolo[1,2−b]phthalazinediones.
- For the synthesis C60 by flash vacuum pyrolysis.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Proline-catalyzed direct asymmetric aldol reactions.
List B, et al.
Journal of the American Chemical Society, 122(10), 2395-2396 (2000)
The direct catalytic asymmetric three-component Mannich reaction.
List B
Journal of the American Chemical Society, 122(38), 9336-9337 (2000)
Zhipeng Zhang et al.
Nature communications, 7, 12478-12478 (2016-08-18)
Due to the high versatility of chiral cyanohydrins, the catalytic asymmetric cyanation reaction of carbonyl compounds has attracted widespread interest. However, efficient protocols that function at a preparative scale with low catalyst loading are still rare. Here, asymmetric counteranion-directed Lewis
Global Trade Item Number
| SKU | GTIN |
|---|---|
| N206-5G-A | 04061834110057 |
| N206-25G-A | 04061834110040 |
| N206-100G-A | 04061832490991 |