4-Bromoindole structure
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Common Name | 4-Bromoindole | ||
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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 | Chinese USA | Flash Point | 145.5±20.4 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 4-bromo-1H-indole |
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Synonym | More Synonyms |
Density | 1.7±0.1 g/cm3 |
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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 |
Storage condition | 0-6°C |
Symbol |
GHS07 |
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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 8 | |
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DownStream 10 | |
HS Code | 2933990090 |
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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% |
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... |
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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... |
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Optically active total synthesis of clavicipitic acid. Yokoyama Y, et al.
J. Org. Chem. 60(6) , 1486-1487, (1995)
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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 |