Identification | More | [Name]
3-Acetylindole | [CAS]
703-80-0 | [Synonyms]
1-(1H-INDOL-3-YL)ETHANONE 3-ACETYL-1-BENZAZOLE 3-ACETYL-2,3-BENZOPYRROLE 3-ACETYLINDOLE 3-INDOLYL METHYL KETONE AKOS BBS-00004490 IFLAB-BB F1727-0313 TIMTEC-BB SBB003977 3-Acetyl-1H-indole Acetyl-3-indole Ketone, indol-3-yl methyl ketone,indol-3-ylmethyl indol-3-yl methyl ketone 3-ACETYLINDOLE PRACTICAL GRADE Ethanone, 1-(1H-indol-3-yl)-(9CI) Ethanone, 1-(1H-indol-3-yl)- 3-Acetylindole ,98% | [EINECS(EC#)]
211-875-5 | [Molecular Formula]
C10H9NO | [MDL Number]
MFCD00005626 | [Molecular Weight]
159.18 | [MOL File]
703-80-0.mol |
Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
OB4520000
| [HazardClass ]
IRRITANT | [HS Code ]
29339990 |
Hazard Information | Back Directory | [Chemical Properties]
yellow to light brown powder | [Uses]
Reactant for preparation of:
- Indole derivatives as antitumor agents
- Endothelin-1 antagonists
- Oncrasin-1 derivatives as inhibitors of the C-terminal domain of RNA polymerase II with antitumor activities
- Inhibitors of hepatitis C NS3/4A serine protease
- Antibacterial agens against MDR Staphylococcus aureus strains
- Antimalarial agents
- Anti-bovine viral diarrhea virus (BVDV) agents
- HIV-1 integrase inhibitors
- Inhibitors of NF-κB transcription regulation related to TNF-α cytokine release
| [Uses]
Reactant for preparation of:• ;Indole derivatives as antitumor agents1• ;Endothelin-1 antagonists2• ;Oncrasin-1 derivatives as inhibitors of the C-terminal domain of RNA polymerase II with antitumor activities3• ;Inhibitors of hepatitis C NS3/4A serine protease4• ;Antibacterial agens against MDR Staphylococcus aureus strains5• ;Antimalarial agents6• ;Anti-bovine viral diarrhea virus (BVDV) agents7• ;HIV-1 integrase inhibitors8• ;Inhibitors of NF-κB transcription regulation related to TNF-α cytokine release9 | [Purification Methods]
Recrystallise the indole from MeOH or *C6H6 containing a little EtOH. The phenylureido derivative has m 154o. [Baker J Chem Soc 461 1946, Beilstein 21/8 V 297.] |
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