About This Item
Produtos recomendados
Nível de qualidade
Ensaio
97%
pf
126-129 °C (lit.)
grupo funcional
bromo
ketone
cadeia de caracteres SMILES
Brc1ccc2C(=O)CCc2c1
InChI
1S/C9H7BrO/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5H,1,4H2
chave InChI
KSONICAHAPRCMV-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
5-Bromo-1-indanone is a 1-indanone derivative. Its physical properties like density, freezing point and refractive index have been determined. It participates in the synthesis of the imidazolyl and triazolyl substituted biphenyl compounds.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral - 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)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Bioorganic & medicinal chemistry letters, 16(2), 378-381 (2005-11-02)
A novel triarylimidazole derivative, SB-590885 (33), bearing a 2,3-dihydro-1H-inden-1-one oxime substituent has been identified as a potent and extremely selective inhibitor of B-Raf kinase.
Journal of medicinal chemistry, 54(12), 4219-4233 (2011-05-12)
Mining of an in-house collection of angiotensin II type 1 receptor antagonists to identify compounds with activity at the peroxisome proliferator-activated receptor-γ (PPARγ) revealed a new series of imidazo[4,5-b]pyridines 2 possessing activity at these two receptors. Early availability of the
Turn-On Fluorogenic Probes for the Selective and Quantitative Detection of the Cyanide Anion from Natural Sources.
Chemistry (Weinheim An Der Bergstrasse, Germany), 8(6), 1271-1278 (2013)
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 229-229 (2015)
Bioorganic & medicinal chemistry, 8(6), 1245-1252 (2000-07-15)
The synthesis of a new series of P450 17 inhibitors is described. The imidazol-1-yl compounds 5 showed strong inhibition of P450 17 rat and especially human enzyme, the most active compounds being 5ax, 5ay and 5bx with IC50 values of
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