About This Item
Fórmula empírica (Notação de Hill):
C8H6BrN
Número CAS:
Peso molecular:
196.04
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
96%
Formulário
solid
pf
41-44 °C (lit.)
grupo funcional
bromo
cadeia de caracteres SMILES
Brc1cccc2cc[nH]c12
InChI
1S/C8H6BrN/c9-7-3-1-2-6-4-5-10-8(6)7/h1-5,10H
chave InChI
RDSVSEFWZUWZHW-UHFFFAOYSA-N
Descrição geral
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.
Aplicação
7-Bromoindole may be used in the synthesis of the following:
- indole
- dyestuffs
- 8-bromocarboline
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
235.4 °F - closed cup
Ponto de fulgor (°C)
113 °C - closed cup
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
Escolha uma das versões mais recentes:
Já possui este produto?
Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
Os clientes também visualizaram
Jin-Hyung Lee et al.
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
Zhiqian Wang et al.
Tetrahedron letters, 53(5), 477-479 (2012-05-01)
A novel MCAP-cycloaddition sequence has been applied to the facile synthesis of β-carboline intermediates to gain rapid access to novel derivatives of yohimbine-like and corynanthe-like compounds that may be easily diversified by cross-coupling reactions and N-derivatizations to generate small compound
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
Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.
Entre em contato com a assistência técnica