CAS 20357-30-6
:(E)-3-(4-bromo-2-nitro-phenyl)prop-2-enoic acid
Description:
(E)-3-(4-bromo-2-nitro-phenyl)prop-2-enoic acid, with CAS number 20357-30-6, is an organic compound characterized by its unique structural features. It contains a prop-2-enoic acid backbone, which is an unsaturated carboxylic acid, and is substituted with a 4-bromo-2-nitrophenyl group. The presence of the bromine and nitro groups introduces significant electron-withdrawing effects, influencing the compound's reactivity and polarity. This compound typically exhibits a yellow to orange color in solid form and is soluble in organic solvents, while its solubility in water may be limited due to the hydrophobic nature of the aromatic ring. The (E) configuration indicates that the substituents on the double bond are on opposite sides, which can affect its biological activity and interaction with other molecules. As a result, this compound may have applications in organic synthesis, medicinal chemistry, or as a potential intermediate in the development of pharmaceuticals. Proper handling and safety precautions are essential due to the presence of halogen and nitro groups, which can pose health and environmental risks.
Formula:C9H6BrNO4
InChI:InChI=1/C9H6BrNO4/c10-7-3-1-6(2-4-9(12)13)8(5-7)11(14)15/h1-5H,(H,12,13)/b4-2+
Synonyms:- (2E)-3-(4-Bromo-2-nitrophenyl)acrylic acid
- 2-propenoic acid, 3-(4-bromo-2-nitrophenyl)-, (2E)-4-Bromo-2-Nitrocinnamic Acid
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50
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100
Found 2 products.
4-Bromo-2-nitrocinnamic acid
CAS:<p>4-Bromo-2-nitrocinnamic acid is a naturally occurring amino acid that is a component of wheat, carrots, and cereals. It is an enzyme inhibitor and has been found to be stable under heat treatment. 4-Bromo-2-nitrocinnamic acid has been shown to inhibit the activity of 3 lysine hydrolase enzymes (LysE1, LysE2, LysE3) in vitro. This inhibition decreases lysine levels and may have health implications for infants fed with 4-bromo-2-nitrocinnamic acid treated wheat flour. The efficiency of 4-bromo-2 nitrocinnamic acid as an enzymatic inhibitor for these enzymes was determined by measuring the release of free lysine from various substrates at different concentrations of the inhibitor. These parameters were then used to calculate the theoretical inhibition percentage for each substrate at a given concentration.</p>Formula:C9H6BrNO4Purity:Min. 95%Molecular weight:272.05 g/mol
