357839
1,5,6,7-Tetrahydro-4H-indol-4-one
98%
Synonym(s):
4,5,6,7-Tetrahydro-4-oxoindole, NSC 131681
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About This Item
Quality Level
Assay
98%
mp
188-190 °C (lit.)
SMILES string
O=C1CCCc2[nH]ccc12
InChI
1S/C8H9NO/c10-8-3-1-2-7-6(8)4-5-9-7/h4-5,9H,1-3H2
InChI key
KASJZXHXXNEULX-UHFFFAOYSA-N
General description
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.
Application
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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