추천 제품
Quality Level
분석
98%
형태
crystals
mp
58-61 °C (lit.)
저장 온도
−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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애플리케이션
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
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
이미 열람한 고객
Chirality, 28(1), 65-71 (2015-10-22)
Chiral O,N,O-tridentate phenol ligands bearing a camphor backbone were found to be effective chiral catalysts for the enantioselective addition of diethylzinc to aromatic aldehydes, resulting in high enantioselectivities (80-95% ee) at room temperature.
A rational chemical synthesis of C60.
Science, 295(5559), 1500-1503 (2002)
Proline-catalyzed direct asymmetric aldol reactions.
Journal of the American Chemical Society, 122(10), 2395-2396 (2000)
The direct catalytic asymmetric three-component Mannich reaction.
Journal of the American Chemical Society, 122(38), 9336-9337 (2000)
An efficient nucleophilic carbene catalyst for the asymmetric benzoin condensation.
Angewandte Chemie (International Edition in English), 41(10), 1743-1745 (2002)
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