1,5,6,7-Tetrahydro-4H-indol-4-one

• Catalog No.: 357839
• CAS Number: 13754-86-4
• M. F.: C8H9NO
• M. W.: 135.16316
• Purity: 98%

SYNONYMS

• Title: 1,5,6,7-四氢-4H-吲哚-4-酮
• IUPAC name: 4,5,6,7-tetrahydro-1H-indol-4-one
• IUPAC Traditional name: 1,5,6,7-tetrahydroindol-4-one
• Synonyms: 4,5,6,7-Tetrahydro-4-oxoindole; NSC 131681

DATABASE IDS

• CAS Number: 13754-86-4
• MDL Number: MFCD00075438
• PubChem SID: 24861947

PROPERTIES

• Empirical Formula (Hill Notation): C8H9NO
• Purity: 98%
• Melting Point: 188-190 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-37/39
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5 g in glass bottle
Application

• Reactant in synthesis of psammopemmin A as antitumor agent1
• Reactant in synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoesters and tricyclic tetrahydrobenzindoles via C-H insertion reactions2
• Reactant in preparation of tricyclic indole and dihydroindole derivatives as inhibitors of guanylate cyclase3
• Reactant in preparation of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of (halobenzyl)pyrroles4
• Reactant in enantioselective preparation of arylalkenyl indoles via asymmetric C-H insertion of rhodium carbenoids followed by Cope rearrangement-elimination5

Description (简体中文)

包装
5 g in glass bottle
Application

• Reactant in synthesis of psammopemmin A as antitumor agent1
• Reactant in synthesis of a 1,3,4,5-tetrahydrobenzindole β-ketoesters and tricyclic tetrahydrobenzindoles via C-H insertion reactions2
• Reactant in preparation of tricyclic indole and dihydroindole derivatives as inhibitors of guanylate cyclase3
• Reactant in preparation of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of (halobenzyl)pyrroles4
• Reactant in enantioselective preparation of arylalkenyl indoles via asymmetric C-H insertion of rhodium carbenoids followed by Cope rearrangement-elimination5