357839
1,5,6,7-Tetrahydro-4H-indol-4-one
98%
Sinonimo/i:
4,5,6,7-Tetrahydro-4-oxoindole, NSC 131681
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
About This Item
Prodotti consigliati
Livello qualitativo
Saggio
98%
Punto di fusione
188-190 °C (lit.)
Gruppo funzionale
ketone
Stringa SMILE
O=C1CCCc2[nH]ccc12
InChI
1S/C8H9NO/c10-8-3-1-2-7-6(8)4-5-9-7/h4-5,9H,1-3H2
KASJZXHXXNEULX-UHFFFAOYSA-N
Descrizione generale
Iodination of 1,5,6,7-tetrahydro-4H-indol-4-one using 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) yields α-iodo derivative as the main product.
Applicazioni
1,5,6,7-Tetrahydro-4H-indol-4-one may be used in the preparation of:
- 4-oxo-4,5,6,7-tetrahydro-1H-indole-2-carbonitrile
- methyl 2-(4-oxo-4,5,6,7-tetrahydro-1H-indol-1-yl)acrylate
- 3-(4-oxo-4,5,6,7-tetrahydro-1H-indol-1-yl)propanenitrile
- potent and orally active 5-HT1A agonists, (R)-(+)- and (S)-(-)-1-formyl-6,7,8,9-tetrahydro-N,N-dipropyl-3H-benz[e]indol-8-amines
- Reactant in synthesis of psammopemmin A as antitumor agent
- Reactant in synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoesters and tricyclic tetrahydrobenzindoles via C-H insertion reactions
- Reactant in preparation of tricyclic indole and dihydroindole derivatives as inhibitors of guanylate cyclase
- Reactant in preparation of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of (halobenzyl)pyrroles
- Reactant in enantioselective preparation of arylalkenyl indoles via asymmetric C-H insertion of rhodium carbenoids followed by Cope rearrangement-elimination
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
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
DNA binders: 1. evaluation of DNA-interactive ability, design, and synthesis of novel intercalating agents
Letters in Drug Design & Discovery, 6(1), 56-62 (2009)
Direct α-iodination of aryl alkyl ketones by elemental iodine activated by 1-chloromethyl-4-fluoro-1, 4-diazoniabicyclo [2.2. 2] octane bis (tetrafluoroborate).
Synthesis, 06, 0853-0858 (2003)
Synthesis of pyrrolo [1, 2-a] indole-1, 8 (5H)-diones as new synthons for developing novel tricyclic compounds of pharmaceutical interest.
ARKIVOC (Gainesville, FL, United States), 5, 97-106 (2004)
Synthesis of (R)-and (S)-1-formyl-6, 7, 8, 9-tetrahydro-N, N-(dipropyl)-3H-benz [e] indol-8-amines: potent and orally active 5-HT1A receptor agonists.
Journal of Heterocyclic Chemistry, 31(1), 129-139 (1994)
Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..
Contatta l'Assistenza Tecnica.