422231
4-(Trifluoromethoxy)benzamidoxime
97%
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About This Item
Fórmula linear:
CF3OC6H4C(=NOH)NH2
Número CAS:
Peso molecular:
220.15
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
97%
pf
113-115 °C (lit.)
grupo funcional
amine
fluoro
oxime
cadeia de caracteres SMILES
N\C(=N/O)c1ccc(OC(F)(F)F)cc1
InChI
1S/C8H7F3N2O2/c9-8(10,11)15-6-3-1-5(2-4-6)7(12)13-14/h1-4,14H,(H2,12,13)
chave InChI
COHKFOZYLCDVRK-UHFFFAOYSA-N
Descrição geral
4-(Trifluoromethoxy)benzamidoxime (4-TFMBAO) is a benzamidoxime (BAO) derivative containing amidoxime functional group. Its density and freezing point have been determined.
Aplicação
4-(Trifluoromethoxy)benzamidoxime (4-TFMBAO) is suitable reactant in the fluorescence (FL) deriving reaction, one of the widely-used methodology specifically used to quantify uracil. It may be used as a reactant in the synthesis of oxadiazoles. It may also be used a fluorogenic agent in the quantification of orotic acid by spectrofluorometric method in human biological specimens.
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)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Sensitive and Selective Determination of Orotic Acid in Biological Specimens Using a Novel Fluorogenic Reaction.
Yin S, et al.
Journal of Fluorescence, 25(4), 1005-1011 (2015)
Thomas E Barta et al.
Bioorganic & medicinal chemistry letters, 21(10), 2820-2822 (2011-04-22)
Seeking compounds preferentially potent and selective for MMP-13, we reported in the preceding Letter on a series of hydroxamic acids with a flexible benzamide tail groups.(1a) Here, we replace the amide moiety with non-hydrolyzable heterocycles in an effort to improve
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 185-185 (2015)
Evan R Abt et al.
Cell chemical biology, 27(2), 197-205 (2019-11-18)
Biosynthesis of the pyrimidine nucleotide uridine monophosphate (UMP) is essential for cell proliferation and is achieved by the activity of convergent de novo and salvage metabolic pathways. Here we report the development and application of a cell-based metabolic modifier screening
Takayuki Shibata et al.
Analytica chimica acta, 674(2), 234-238 (2010-08-04)
Facile and specific methods to quantify a nucleobase in biological samples are of great importance for diagnosing disorders in nucleic acid metabolism. In the present study, a novel fluorogenic reaction specific for uracil has been developed. The reaction was carried
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