6-bromoindole
Names
[ CAS No. ]:
52415-29-9
[ Name ]:
6-bromoindole
[Synonym ]:
6-brom-1H-indole
6-BROMINDOL
6-Bromoindole
bromoindole-6
1H-Indole, 6-bromo-
6-Bromo-1H-indole
6-bromo-1 H-indole
MFCD00238550
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
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
MSDS
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
Synthetic Route
Precursor & DownStream
Precursor
DownStream
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%
Articles
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...