473723
7-Bromoindole
96%
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About This Item
Formule empirique (notation de Hill):
C8H6BrN
Numéro CAS:
Poids moléculaire :
196.04
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
96%
Forme
solid
Pf
41-44 °C (lit.)
Chaîne SMILES
Brc1cccc2cc[nH]c12
InChI
1S/C8H6BrN/c9-7-3-1-2-6-4-5-10-8(6)7/h1-5,10H
Clé InChI
RDSVSEFWZUWZHW-UHFFFAOYSA-N
Description générale
7-Bromoindole is a 7-substituted indole derivative. Its synthesis from 7-bromoindole-2-carboxylic acid has been reported. It has been reported to reduce the production of staphyloxanthin in Staphylococcus aureus.
Application
7-Bromoindole may be used in the synthesis of the following:
- indole
- dyestuffs
- 8-bromocarboline
Mention d'avertissement
Warning
Mentions de danger
Conseils de prudence
Classification des risques
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organes cibles
Respiratory system
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
235.4 °F - closed cup
Point d'éclair (°C)
113 °C - closed cup
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Les clients ont également consulté
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Applied microbiology and biotechnology, 97(10), 4543-4552 (2013-01-16)
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 virulence without affecting cell viability and thus, may not lead to drug resistance. Staphylococcus aureus
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Tetrahedron letters, 53(5), 477-479 (2012-05-01)
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The structure of monobrominated ethyl indole-3-carboxylate and the preparation of 7-bromoindole.
Leggetter BE and Brown RK.
Canadian Journal of Chemistry, 38(9), 1467-1471 (1960)
Total synthesis of indoles from Tricholoma species via Bartoli/heteroaryl radical methodologies.
A Dobbs
The Journal of organic chemistry, 66(2), 638-641 (2001-06-30)
J Y Kim et al.
Letters in applied microbiology, 41(2), 163-168 (2005-07-22)
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 Pseudomonas sp. KL33, which possesses a phenol degradation pathway similar to that found in
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