All Photos(4)
About This Item
Linear Formula:
C10H7CHO
CAS Number:
Molecular Weight:
156.18
Beilstein:
507750
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
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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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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The direct catalytic asymmetric three-component Mannich reaction.
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Journal of the American Chemical Society, 122(38), 9336-9337 (2000)
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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
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An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
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Angewandte Chemie (International Edition in English), 41(10), 1743-1745 (2002)
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