CAS 52415-29-9|6-bromoindole
Introduction：Basic information about CAS 52415-29-9|6-bromoindole, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| 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 | ChineseUSA | Flash Point | 145.5±20.4 °C |
| Symbol | GHS07 | Signal Word | Warning |
Names
| Name | 6-bromo-1H-indole |
|---|---|
| Synonym | More Synonyms |
6-bromoindole BiologicalActivity
| 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 | Research Areas >>Others |
| In Vitro | 6-溴吲哚试剂 |
Chemical & Physical Properties
| 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 |
| InChIKey | MAWGHOPSCKCTPA-UHFFFAOYSA-N |
| SMILES | Brc1ccc2cc[nH]c2c1 |
Safety Information
| 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 |
Customs
| 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% |
Articles8
More Articles| 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... |
Synonyms
| 6-brom-1H-indole |
| 6-BROMINDOL |
| 6-Bromoindole |
| bromoindole-6 |
| 1H-Indole, 6-bromo- |
| 6-Bromo-1H-indole |
| 6-bromo-1 H-indole |
| MFCD00238550 |
