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7-Bromo-1H-indole

Names

[ CAS No. ]:
51417-51-7

[ Name ]:
7-Bromo-1H-indole

[Synonym ]:
7-Bromoindole
1H-Indole,7-broMo
3-CYANO-7-CHLORO INDOLE
7-bromoidnole
7-Brom-indol
7-BROMOCHROMANONE
7-bromo indole
MFCD00799492
1H-Indole, 7-bromo-
7-Bromo-1H-indole
7-broMo-4H-indole
7-BroMoindole 250MG
RARECHEM AH BS 0083

Biological Activity

[Description]:

7-Bromo-1H-indole 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

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
316.9±15.0 °C at 760 mmHg

[ Melting Point ]:
41-44 °C(lit.)

[ 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

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 ]:
Xn:Harmful

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S36-S36/37/39-S22

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29339990

Synthetic Route

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

Multicomponent phenol hydroxylase-catalysed formation of hydroxyindoles and dyestuffs from indole and its derivatives.

Lett. Appl. Microbiol. 41(2) , 163-8, (2005)

To establish multicomponent phenol hydroxylases (mPHs) as novel biocatalysts for producing dyestuffs and hydroxyindoles such as 7-hydroxyindole (7-HI) from indole and its derivatives.We have isolated ...

Indole and 7-benzyloxyindole attenuate the virulence of Staphylococcus aureus.

Appl. Microbiol. Biotechnol. 97(10) , 4543-52, (2013)

Human pathogens can readily develop drug resistance due to the long-term use of antibiotics that mostly inhibit bacterial growth. Unlike antibiotics, antivirulence compounds diminish bacterial virulen...

Diversity Oriented Synthesis: Concise Entry to Novel Derivatives of Yohimbine and Corynanthe Alkaloids.

Tetrahedron Lett. 53(5) , 477-479, (2012)

A novel MCAP-cycloaddition sequence has been applied to the facile synthesis of _-carboline intermediates to gain rapid access to novel derivatives of yohimbine-like and corynanthe-like compounds that...


More Articles


Related Compounds

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