3-Acetylindole
3-Acetylindole Basic information
- Product Name:
- 3-Acetylindole
- Synonyms:
-
- TIMTEC-BB SBB003977
- IFLAB-BB F1727-0313
- 3-ACETYL-2,3-BENZOPYRROLE
- 3-ACETYL-1-BENZAZOLE
- 3-ACETYLINDOLE
- 3-INDOLYL METHYL KETONE
- 1-(1H-INDOL-3-YL)ETHANONE
- AKOS BBS-00004490
- CAS:
- 703-80-0
- MF:
- C10H9NO
- MW:
- 159.18
- EINECS:
- 211-875-5
- Product Categories:
-
- Building Blocks
- C10
- Simple Indoles
- Pyrroles & Indoles
- Chemical Synthesis
- Heterocyclic Building Blocks
- ACETYLGROUP
- Indoles and derivatives
- IndoleDerivative
- Pyrroles & Indoles
- Indole
- Heterocyclic Compounds
- Indoles
- Mol File:
- 703-80-0.mol
3-Acetylindole Chemical Properties
- Melting point:
- 188-192 °C (lit.)
- Boiling point:
- 284.68°C (rough estimate)
- Density
- 1.1202 (rough estimate)
- refractive index
- 1.6070 (estimate)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- DMSO; Dichloromethane; Methanol;
- form
- Powder
- pka
- 15.38±0.30(Predicted)
- color
- Yellow to light brown
- BRN
- 122579
- CAS DataBase Reference
- 703-80-0(CAS DataBase Reference)
- NIST Chemistry Reference
- Ethanone, 1-(1h-indol-3-yl)-(703-80-0)
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
- RTECS
- OB4520000
- HazardClass
- IRRITANT
- HS Code
- 29339990
MSDS
- Language:English Provider:3-Acetylindole
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
3-Acetylindole Usage And Synthesis
Chemical Properties
yellow to light brown powder
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
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
3-Acetylindole can be used as anti-fungal agents.
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.]
3-AcetylindoleSupplier
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3-Acetylindole(703-80-0)Related Product Information
- Indole-3-acetic acid
- Indometacin
- Indole-3-butyric acid
- Methyl indolyl-3-glyoxylate
- (2-METHYL-1H-INDOL-3-YL)-OXO-ACETIC ACID ETHYL ESTER
- (1H-INDOL-3-YL)-OXO-ACETIC ACID ETHYL ESTER
- Indole-3-glyoxylic acid
- INDOLE-3-GLYOXYLAMIDE
- INDOLE-3-GLYOXYLYL CHLORIDE
- 1,3-DIACETYLINDOLE
- N-ACETYLINDOLE-3-CARBOXALDEHYDE,l-acetylindole-3-carboxaldehyde,N-ACETYLINDOLE-3-ALDEHYDE,1-ACETYLINDOLE-3-CARBOXALDEHYDE,1-ACETYLINDOLE-3-CARBALDEHYDE
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- N-ACETYLINDOLE,Acetylindole,L-Acetylindole,1-ACETYLINDOLE
- 3-dimethylamino-1-(1H-indol-3-yl)propan-1-one
- N,N-Dipropyl-3-indoleglyoxylamide
- 1-(1H-INDOL-3-YL)-PROPAN-1-ONE
- 5-BENZYLOXYINDOLE-3-GLYOXYLAMIDE