422231
4-(Trifluoromethoxy)benzamidoxime
97%
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About This Item
Formule linéaire :
CF3OC6H4C(=NOH)NH2
Numéro CAS:
Poids moléculaire :
220.15
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
97%
Pf
113-115 °C (lit.)
Groupe fonctionnel
amine
fluoro
oxime
Chaîne 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)
Clé InChI
COHKFOZYLCDVRK-UHFFFAOYSA-N
Description générale
4-(Trifluoromethoxy)benzamidoxime (4-TFMBAO) is a benzamidoxime (BAO) derivative containing amidoxime functional group. Its density and freezing point have been determined.
Application
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.
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)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
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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