6-bromoindole

Modify Date: 2024-01-02 16:48:41

6-bromoindole Structure
6-bromoindole structure
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 Chinese USA Flash Point 145.5±20.4 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 6-bromoindole


6-Bromoindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 6-bromo-1H-indole
Synonym More Synonyms

 6-bromoindole 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
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

 Safety Information

Symbol GHS07
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

 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
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