6-bromoindole structure 
             | 
        Common Name | 6-bromoindole | ||
|---|---|---|---|---|
| CAS Number | 52415-29-9 | Molecular Weight | 196.04 | |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 316.9±15.0 °C at 760 mmHg | |
| Molecular Formula | C8H6BrN | Melting Point | 92-96 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 145.5±20.4 °C | |
| Symbol | 
             
            
            GHS07  | 
        Signal Word | Warning | |
            Use of 6-bromoindole6-Bromoindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.  | 
    
| Name | 6-bromo-1H-indole | 
|---|---|
| Synonym | More Synonyms | 
| Description | 6-Bromoindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | 
|---|---|
| Related Catalog | |
| In Vitro | 6-溴吲哚试剂 | 
| Density | 1.7±0.1 g/cm3 | 
|---|---|
| Boiling Point | 316.9±15.0 °C at 760 mmHg | 
| Melting Point | 92-96 °C(lit.) | 
| Molecular Formula | C8H6BrN | 
| Molecular Weight | 196.04 | 
| Flash Point | 145.5±20.4 °C | 
| Exact Mass | 194.968353 | 
| PSA | 15.79000 | 
| LogP | 2.91 | 
| Vapour Pressure | 0.0±0.7 mmHg at 25°C | 
| Index of Refraction | 1.712 | 
| 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-S37/39 | 
| RIDADR | NONH for all modes of transport | 
| WGK Germany | 3 | 
| HS Code | 2942000000 | 
| Precursor 8 | |
|---|---|
| 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% | 
| 
                                    
                                    Indoline derivatives as 5-HT(2C) receptor agonists.
                                    
                                    
                                     Bioorg. Med. Chem. Lett. 14 , 2367-2370, (2004) A series of 1-(1-indolinyl)-2-propylamines was synthesised and evaluated as 5-HT(2C) receptor agonists for the treatment of obesity. The general methods of synthesis of the precursor indoles are descr...  | 
                                |
| 
                                    
                                    Synthesis and biological evaluation of achiral indole-substituted titanocene dichloride derivatives.
                                    
                                    
                                     Int J Med Chem 2012 , 905981, (2015) Six new titanocene compounds have been isolated and characterised. These compounds were synthesised from their fulvene precursors using Super Hydride (LiBEt3H) followed by transmetallation with titani...  | 
                                |
| 
                                    
                                    Enantioselective total syntheses of (+)-arborescidine A, (-)-arborescidine B, and (-)-arborescidine C.
                                    
                                    
                                     J. Org. Chem. 69 , 1283-1289, (2004) Described are the first enantioselective total syntheses of (+)-arborescidine A ((+)-1), (-)-arborescidine B ((-)-2), and (-)-arborescidine C ((-)-3), via routes that proceeded in five steps and 50% o...  | 
                                
| 6-brom-1H-indole | 
| 6-BROMINDOL | 
| 6-Bromoindole | 
| bromoindole-6 | 
| 1H-Indole, 6-bromo- | 
| 6-Bromo-1H-indole | 
| 6-bromo-1 H-indole | 
| MFCD00238550 |