CAS 5041-33-8
:Carbamic acid, 2-propenyl-, phenylmethyl ester
Description:
Carbamic acid, 2-propenyl-, phenylmethyl ester, with the CAS number 5041-33-8, is an organic compound that belongs to the class of carbamates. This substance features a carbamic acid moiety where the hydrogen of the carboxyl group is replaced by a 2-propenyl group and a phenylmethyl (benzyl) group. It is typically characterized by its ester functional group, which contributes to its reactivity and potential applications in organic synthesis. The compound may exhibit moderate solubility in organic solvents and is likely to be less soluble in water due to its hydrophobic aromatic components. Its structure suggests potential uses in the synthesis of pharmaceuticals, agrochemicals, or as an intermediate in various chemical reactions. As with many carbamates, it may also possess biological activity, which could be of interest in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as carbamates can vary in toxicity and environmental impact.
Formula:C11H13NO2
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Found 3 products.
Allylamine, N-CBZ protected
CAS:Allylamine, N-CBZ protectedPurity:≥95%Color and Shape:LiquidMolecular weight:191.22642g/molBenzyl allylcarbamate
CAS:Benzyl allylcarbamate is a potent inhibitor of enzymes. It is an inhibitor of the enzyme CYP2E1 and prevents the formation of reactive oxygen species (ROS) in cells. Benzyl allylcarbamate also has anti-inflammatory properties that are due to its ability to inhibit the production of pro-inflammatory cytokines such as tumor necrosis factor-α (TNF-α). This drug has been shown to be effective against atherosclerotic lesions in mice and congestive heart failure in rats. The biological properties of benzyl allylcarbamate have been studied extensively, including its effects on allergic responses and Alzheimer's disease.
Formula:C11H13NO2Purity:Min. 95%Molecular weight:191.23 g/mol
