513830
Indole-5-carboxaldehyde
98%
Sinonimo/i:
5-Formylindole
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Cambia visualizzazione
5 G
CHF 44.30
About This Item
Formula empirica (notazione di Hill):
C9H7NO
Numero CAS:
Peso molecolare:
145.16
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
98%
Punto di fusione
100-103 °C (lit.)
Gruppo funzionale
aldehyde
Stringa SMILE
O=Cc1ccc2[nH]ccc2c1
InChI
1S/C9H7NO/c11-6-7-1-2-9-8(5-7)3-4-10-9/h1-6,10H
ADZUEEUKBYCSEY-UHFFFAOYSA-N
Categorie correlate
Applicazioni
Indole-5-carboxaldehyde can be used as a reactant in the:
- Preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents[1]
- Preparation of analogs of botulinum neurotoxin serotype A protease inhibitors[2]
- Stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes[3]
- Synthesis of para-para stilbenophanes by McMurry coupling[4]
- Stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes[5]
- Structure-based drug design of aurora kinase A inhibitors[6]
- Preparation of 5-indolyl linked 15- and 18-membered azacrown ethers to study their cation-π interactions.[7]
- Preparation of bibenzimidazole derivatives substituted 5-indolyl moiety in the study of inhibition of topoisomerase I activity.[8]
- Synthesis of (5-(4-(3,4,5-trimethoxybenzoyl)-1H-imidazol-2-yl)-1H-indol-2-yl)(3,4,5-trimethoxyphenyl)methanone[9] and radioiodinated indolochalcone.[10]
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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