5-Fluoroindole structure
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Common Name | 5-Fluoroindole | ||
|---|---|---|---|---|
| CAS Number | 399-52-0 | Molecular Weight | 135.14 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 258.0±13.0 °C at 760 mmHg | |
| Molecular Formula | C8H6FN | Melting Point | 45-48 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 109.9±19.8 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of 5-Fluoroindole5-Fluoroindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | 5-fluoroindole |
|---|---|
| Synonym | More Synonyms |
| Description | 5-Fluoroindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 258.0±13.0 °C at 760 mmHg |
| Melting Point | 45-48 °C(lit.) |
| Molecular Formula | C8H6FN |
| Molecular Weight | 135.14 |
| Flash Point | 109.9±19.8 °C |
| Exact Mass | 135.048431 |
| PSA | 15.79000 |
| LogP | 2.28 |
| Vapour Pressure | 0.0±0.5 mmHg at 25°C |
| Index of Refraction | 1.646 |
| InChIKey | ODFFPRGJZRXNHZ-UHFFFAOYSA-N |
| SMILES | Fc1ccc2[nH]ccc2c1 |
| Storage condition | 2-8°C |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xi:Irritant |
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26-S36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2933990090 |
| Precursor 9 | |
|---|---|
| DownStream 10 | |
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Ionization potentials of fluoroindoles and the origin of nonexponential tryptophan fluorescence decay in proteins.
J. Am. Chem. Soc. 127(11) , 4104-13, (2005) This work reports an explanation for the unusual monoexponential fluorescence decay of 5-fluorotryptophan (5FTrp) in single-Trp mutant proteins [Broos, J.; Maddalena, F.; Hesp, B. H. J. Am. Chem. Soc.... |
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Regulation of tryptophan synthase gene expression in Chlamydia trachomatis.
Mol. Microbiol. 49(5) , 1347-59, (2003) We previously reported that Chlamydia trachomatis expresses the genes encoding tryptophan synthase (trpA and trpB). The results presented here indicate that C. trachomatis also expresses the tryptopha... |
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Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography.
J. Med. Chem. 52 , 4694-715, (2009) We describe a novel fragment library termed fragments of life (FOL) for structure-based drug discovery. The FOL library includes natural small molecules of life, derivatives thereof, and biaryl protei... |
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Name: Inhibition of peptidase activity of human recombinant LTA4H expressed in Escherichia ...
Source: ChEMBL
Target: Leukotriene A-4 hydrolase
External Id: CHEMBL1032963
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Name: Inhibition of hydrolase activity of human recombinant LTA4H expressed in Escherichia ...
Source: ChEMBL
Target: Leukotriene A-4 hydrolase
External Id: CHEMBL1032964
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Name: Experimentally measured binding affinity data (IC50) for protein-ligand complexes der...
Source: Shanghai Institute of Organic Chemistry
Target: N/A
External Id: PDBbind-IC50 for protein-ligand complexes
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Name: Inhibition of ionomycin-stimulated LTB4 production in human whole blood treated 15 mi...
Source: ChEMBL
Target: Blood
External Id: CHEMBL1032965
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| MFCD00005671 |
| 5-Fluoro-1H-indole |
| 5-Fluoroindole |
| 5-Fluoro indole |
| EINECS 206-917-4 |