CAS 52488-36-5|4-Bromoindole
Introduction：Basic information about CAS 52488-36-5|4-Bromoindole, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | 4-Bromoindole | ||
|---|---|---|---|
| CAS Number | 52488-36-5 | Molecular Weight | 196.044 |
| Density | 1.7±0.1 g/cm3 | Boiling Point | 316.9±15.0 °C at 760 mmHg |
| Molecular Formula | C8H6BrN | Melting Point | 17 °C |
| MSDS | ChineseUSA | Flash Point | 145.5±20.4 °C |
| Symbol | GHS07 | Signal Word | Warning |
Names
| Name | 4-bromo-1H-indole |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.7±0.1 g/cm3 |
|---|---|
| Boiling Point | 316.9±15.0 °C at 760 mmHg |
| Melting Point | 17 °C |
| Molecular Formula | C8H6BrN |
| Molecular Weight | 196.044 |
| 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 | GRJZJFUBQYULKL-UHFFFAOYSA-N |
| SMILES | Brc1cccc2[nH]ccc12 |
| Storage condition | 0-6°C |
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 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2933990090 |
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% |
Articles4
More Articles| A concise and scalable strategy for the total synthesis of dictyodendrin B based on sequential C-H functionalization. Angew. Chem. Int. Ed. Engl. 54(18) , 5451-5, (2015) A sequential CH functionalization strategy for the synthesis of the marine alkaloid dictyodendrin B is reported. Our synthesis begins from commercially available 4-bromoindole and involves six direct... | |
| Applications of vinylogous Mannich reactions. Total syntheses of the Ergot alkaloids rugulovasines A and B and setoclavine. J. Am. Chem. Soc. 123(25) , 5918-24, (2001) Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b), and setoclavine (2) have been completed by strategies that feature inter- and intramolecular vinylogous Mannich react... | |
| Optically active total synthesis of clavicipitic acid. Yokoyama Y, et al. J. Org. Chem. 60(6) , 1486-1487, (1995) |
Synonyms
| 5-Br-indole |
| 4-bromo-indole |
| 5-Bromo-1H-indole |
| 5-bromo-indole |
| 4-bromindole |
| MFCD00671502 |
| 5-BI |
| 1H-INDOLE,4-BROMO |
| 4-Bromo-1H-indole |
| 5-broMo-2H-indole |
| 1H-Indole, 4-bromo- |
| 1H-Indole, 5-bromo- |
| 5-bromonindole |
| 5-Bromide indole |
| 5-indolyl bromide |
| 4-Brom-indol |
| 5-Bromindole |
| 4-Bromoindole |
| 5-Bromoindole |
| Bromoindole |
