Identification | More | [Name]
6-Fluoroindole | [CAS]
399-51-9 | [Synonyms]
1H-INDOLE, 6-FLUORO- 6-FLUORO-1H-INDOLE 6-FLUOROINDOLE BUTTPARK 24\07-34 6-Fluoroindole98% 6-FLUORO-2-IODOBENZALDEHYDE | [EINECS(EC#)]
700-113-1 | [Molecular Formula]
C8H6FN | [MDL Number]
MFCD00056933 | [Molecular Weight]
135.14 | [MOL File]
399-51-9.mol |
Chemical Properties | Back Directory | [Appearance]
beige-brown crystalline powder | [Melting point ]
72-76 °C (lit.) | [Boiling point ]
230°C (rough estimate) | [density ]
1.1203 (estimate) | [storage temp. ]
2-8°C
| [form ]
Crystalline Powder | [pka]
16.40±0.30(Predicted) | [color ]
Beige-brown | [Water Solubility ]
Insoluble | [Sensitive ]
Light Sensitive | [Detection Methods]
HPLC,NMR | [BRN ]
112192 | [InChI]
InChI=1S/C8H6FN/c9-7-2-1-6-3-4-10-8(6)5-7/h1-5,10H | [InChIKey]
YYFFEPUCAKVRJX-UHFFFAOYSA-N | [SMILES]
N1C2=C(C=CC(F)=C2)C=C1 | [CAS DataBase Reference]
399-51-9(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [F ]
10 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29339900 |
Hazard Information | Back Directory | [Chemical Properties]
beige-brown crystalline powder | [Uses]
6-Fluoroindole acts as a reagent in the synthesis of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles, which acts as a potential anticancer immunomodulator. It is also employed as an antifungal and antibacterial agent. Further, it serves as a potent selective serotonin reuptake inhibitor. In addition to this, it is used as a inhibitor of HIV-1 attachment. | [General Description]
6-Fluoroindole is a halogen substituted indole. Experimental ionization potential of 6-fluoroindole has been evaluated. Preparation of 6-fluoroindole via nitration of indoline has been reported. |
|
|