CAS 67706-68-7
:Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, ethylester
Description:
Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, ethyl ester, identified by CAS number 67706-68-7, is an organic compound characterized by its ester functional group and a butanoic acid backbone. This compound features a butanoic acid moiety, which contributes to its fatty acid characteristics, while the ethyl ester group enhances its solubility in organic solvents. The presence of the 1,1-dimethylethoxycarbonyl group indicates that it has a bulky substituent, which can influence its reactivity and steric properties. Typically, such compounds exhibit moderate to low toxicity and are used in various chemical syntheses, including pharmaceuticals and agrochemicals. The compound may also display properties such as being a potential intermediate in organic synthesis, with applications in the development of more complex molecules. Its stability, solubility, and reactivity can vary based on environmental conditions, such as pH and temperature, making it important to consider these factors in practical applications.
Formula:C11H19NO5
Synonyms:- 4-(Boc-amino)-3-oxobutanoic acid ethyl ester
- TERT-BUTYL 3-(ETHOXYCARBONYL)-2-OXOPROPYLCARBAMATE
- 132862
- 4-[(tert-Butoxycarbonyl)amino]-3-oxobutanoic acid ethyl ester
- Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, ethyl ester
- Ethyl 4-((tert-butoxycarbonyl)aMino)-3-oxobutanoate
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Found 4 products.
4-[(tert-Butoxycarbonyl)amino]-3-oxobutanoic acid ethyl ester
CAS:Formula:C11H19NO5Purity:95%Color and Shape:LiquidMolecular weight:245.2723Ethyl 4-((tert-butoxycarbonyl)amino)-3-oxobutanoate
CAS:Ethyl 4-((tert-butoxycarbonyl)amino)-3-oxobutanoatePurity:95%Molecular weight:245.27g/molethyl 4-[(tert-butoxycarbonyl)amino]-3-oxobutanoate
CAS:Formula:C11H19NO5Purity:95%Color and Shape:LiquidMolecular weight:245.275Ethyl 4-[(tert-Butoxycarbonyl)amino]-3-oxobutanoate
CAS:<p>Ethyl 4-[(tert-Butoxycarbonyl)amino]-3-oxobutanoate (4BAA) is a synthetic compound that has been shown to have anticancer activity in vitro. It reversibly inhibits DNA synthesis and cell proliferation by inhibiting the enzymatic activity of DNA polymerase II and topoisomerase II. 4BAA also has an inhibitory effect on the proliferation of tumor cells, which may be due to its ability to inhibit protein synthesis. In vivo studies have shown that this compound accumulates in tumor tissue, but not in normal tissues, at concentrations that are 10-fold higher than those found in plasma. This agent also inhibits the growth of fibroblasts and other non-malignant cells in vitro.</p>Formula:C11H19NO5Purity:Min. 95%Molecular weight:245.27 g/mol



