6-bromoindole

Names

[ 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]:

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

MSDS

Click to get detail 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

Click to get detail 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

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...