ChemicalBook >> CAS DataBase List >>6-Fluoroindole

6-Fluoroindole

CAS No.
399-51-9
Chemical Name:
6-Fluoroindole
Synonyms
6-FLUORO-1H-INDOLE;6-FL;uoroindoL;NSC 520436;6-FLUOROINDOLE;6-Fluro-1H-indole;BUTTPARK 24\07-34;6-Fluoroindole98%;6-Fluoroindole>6-Fluoroindole 98%
CBNumber:
CB1772999
Molecular Formula:
C8H6FN
Molecular Weight:
135.14
MDL Number:
MFCD00056933
MOL File:
399-51-9.mol
MSDS File:
SDS
Last updated:2026-05-27 23:45:02
Product description Number Pack Size Price
6-Fluoroindole 98% 349593 5g $82.4
6-Fluoroindole 98% 349593 1g $42.5
6-Fluoroindole >98.0%(GC) F0352 1g $34
6-Fluoroindole >98.0%(GC) F0352 5g $103
6-Fluoroindole 98+% ≥98% 234713 1g $156
More product size

6-Fluoroindole Properties

Melting point 72-76 °C (lit.)
Boiling point 230°C (rough estimate)
Density 1.1203 (estimate)
Flash point >110°
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Crystalline Powder
pka 16.40±0.30(Predicted)
color Beige-brown
Water Solubility Insoluble
Sensitive Light Sensitive
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)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
10
HazardClass  IRRITANT
HS Code  29339900
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

6-Fluoroindole price More Price(106)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 349593 6-Fluoroindole 98% 399-51-9 5g $82.4 2026-04-30 Buy
Sigma-Aldrich 349593 6-Fluoroindole 98% 399-51-9 1g $42.5 2023-06-20 Buy
TCI Chemical F0352 6-Fluoroindole >98.0%(GC) 399-51-9 1g $34 2026-04-30 Buy
TCI Chemical F0352 6-Fluoroindole >98.0%(GC) 399-51-9 5g $103 2026-04-30 Buy
Usbiological 234713 6-Fluoroindole 98+% ≥98% 1g $156 2026-06-03 Buy
Product number Packaging Price Buy
349593 5g $82.4 Buy
349593 1g $42.5 Buy
F0352 1g $34 Buy
F0352 5g $103 Buy
234713 1g $156 Buy

6-Fluoroindole Chemical Properties,Uses,Production

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.

Synthesis

Hydrazinecarboxamide, 2-[2-(4-fluoro-2-nitrophenyl)ethylidene]-, (2E)-

1065183-63-2

6-Fluoroindole

399-51-9

The general procedure for the synthesis of 6-fluoroindole from the compound (CAS: 1065183-63-2) is as follows: Intermediate 110: Synthesis of 6-fluoro-1H-indole. In a 1 L high-pressure reactor, (4-fluoro-2-nitrophenyl)acetaldehyde semicarbazone (27.0 g, 0.110 mol) was suspended in THF (750 mL) with stirring. To this suspension was added a slurry of Rh/C (5 wt%) in toluene and Fe(OAc)2 (2.9 g, 0.017 mol), where the amount of Rh was 3.5 g, 0.002 mol. The reactor was charged with H2 to 50 atm and the reaction was stirred for 2 days at room temperature. After completion of the reaction, the mixture was filtered through a diatomaceous earth pad and washed with MeOH (150 mL). The filtrate was concentrated to give a black oil, which was partitioned between DCM (500 mL) and water (300 mL). The organic layer was separated and the aqueous phase was extracted with DCM (2 x 200 mL). The organic phases were combined, washed with brine (200 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was dissolved in DCM (100 mL) and decolorized by a fast silica gel column. After filtration, the filtrate was concentrated under reduced pressure to give 12.9 g (87% yield) of 6-fluoroindole. 1H NMR (300 MHz, DMSO-d6) δ: 11.11 (1H, s), 7.49 (1H, dd, J = 8.6, 5.5 Hz), 7.30 (1H, t, J = 2.4 Hz), 7.13 (1H, dd, J = 10.3, 2.4 Hz), 6.81 (1H, ddd, J = 11.0, 7.6, 2.4 Hz), 6.40-6.38 (1H, m).

References

[1] Patent: WO2008/118724, 2008, A1. Location in patent: Page/Page column 126

1065183-63-2
399-51-9
Synthesis of 6-Fluoroindole from Hydrazinecarboxamide, 2-[2-(4-fluoro-2-nitrophenyl)ethylidene]-, (2E)-
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View Lastest Price from 6-Fluoroindole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
6-Fluoroindole pictures 2026-02-02 6-Fluoroindole
399-51-9
5mg 99%HPLC 2000tons Shaanxi Dideu Medichem Co. Ltd
1-Methyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine dihydrochloride pictures 2026-02-02 1-Methyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine dihydrochloride
399-51-9
5mg 99%HPLC 2000tons Shaanxi Dideu Medichem Co. Ltd
6-Fluoroindole pictures 2026-01-29 6-Fluoroindole
399-51-9
1g 98% 30kg LAURENT
6-FLUORO-2-IODOBENZALDEHYDE 6-Fluoroindole in stock Factory 6-FL uoroindoL 6-FLUOROINDOLE FOR SYNTHESIS 25 G 6-FLUOROINDOLE FOR SYNTHESIS 5 G 6-Fluoroindole ,97% 6-Fluoroindole,6-Fluoro-1H-indole 6-Fluro-1H-indole 6 - fluorine indole NSC 520436 6-Fluoroindole 98% 6-FLUOROINDOLE 1H-INDOLE, 6-FLUORO- BUTTPARK 24\07-34 6-Fluoroindole98% 6-Fluoroindole> 6-FLUORO-1H-INDOLE 399-51-9 339-51-9 Heterocyclic Building Blocks FA - FL Alphabetic Indoles Simple Indoles Analytical Chromatography Product Catalog Building Blocks Analytical Standards Indole Series Simple Indoles Indole FA - FLBuilding Blocks Alphabetic F Heterocyclic Building Blocks Building Blocks Indoles blocks FluoroCompounds IndolesOxindoles Indole/indoline/oxindole Indole and Indoline Indoles and derivatives bc0001