CAS 42116-44-9
:Carbamic acid, (phenylmethyl)-, 1,1-dimethylethyl ester
Description:
Carbamic acid, (phenylmethyl)-, 1,1-dimethylethyl ester, with the CAS number 42116-44-9, is an organic compound characterized by its ester functional group derived from carbamic acid. This compound features a phenylmethyl group, which contributes to its aromatic properties, and a tert-butyl group, which enhances its steric bulk. The presence of these groups suggests that the compound may exhibit moderate to low polarity, influencing its solubility in various solvents. Typically, esters like this one are known for their pleasant odors and are often used in flavoring and fragrance applications. The compound may also participate in various chemical reactions, such as hydrolysis, under appropriate conditions. Its stability and reactivity can be affected by environmental factors such as temperature and pH. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards. Overall, this compound represents a unique structure within the class of carbamates, with potential applications in organic synthesis and industrial chemistry.
Formula:C12H17NO2
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Found 5 products.
Carbamic acid, (phenylmethyl)-, 1,1-dimethylethyl ester
CAS:Formula:C12H17NO2Purity:98%Color and Shape:SolidMolecular weight:207.2689tert-Butyl Benzylcarbamate
CAS:Formula:C12H17NO2Purity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:207.27N-Boc-Benzylamine
CAS:Formula:C12H17NO2Purity:98%Color and Shape:Solid, Low Melting SolidMolecular weight:207.273tert-Butyl N-benzylcarbamate
CAS:Tert-Butyl N-benzylcarbamate is a synthetic compound that is being developed for the treatment of cancer. It is an analog of carmustine, a drug used for the treatment of brain tumors, and has been shown to be effective against cell lines in vitro. Tert-Butyl N-benzylcarbamate binds to DNA and inhibits protein synthesis, leading to cancer cell death. The drug also inhibits the growth of cancer cells by inhibiting chloride channels and blocking the influx of hydrogen chloride into cells. Tert-Butyl N-benzylcarbamate has not been tested in humans yet, but it has shown promising results in animal models.Formula:C12H17NO2Purity:Min. 95%Molecular weight:207.27 g/mol




