
CAS 66494-26-6
:methyl 1-(tert-butoxycarbonylaMino)cyclopropanecarboxylate
Description:
Methyl 1-(tert-butoxycarbonylamino)cyclopropanecarboxylate, identified by its CAS number 66494-26-6, is a chemical compound that features a cyclopropane ring, which is a three-membered carbon structure known for its unique strain and reactivity. This compound contains a methyl ester functional group, contributing to its reactivity and solubility characteristics. The presence of a tert-butoxycarbonyl (Boc) group indicates that it is likely used in organic synthesis, particularly in the protection of amines during chemical reactions. The Boc group is a common protective group in peptide synthesis, allowing for selective reactions without interfering with the amine functionality. Methyl 1-(tert-butoxycarbonylamino)cyclopropanecarboxylate may exhibit moderate polarity due to the ester and amine functionalities, influencing its solubility in various organic solvents. Additionally, the compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals that target specific biological pathways. Overall, its unique structural features and functional groups make it a valuable compound in synthetic organic chemistry.
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
Methyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
CAS:Formula:C10H17NO4Purity:97%Color and Shape:SolidMolecular weight:215.2463Methyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
CAS:<p>Methyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate</p>Purity:97%Molecular weight:215.25g/molMethyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
CAS:Purity:97%Molecular weight:215.2489929Methyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
CAS:<p>Methyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate is a six-membered analogue of the five-membered ring compound iprodione. It is used in the synthesis of compounds that are used as fungicides, such as propiconazole and fenpropimorph. This chemical reacts with nucleophiles to form adducts, which can be isolated in high yield by chromatography or crystallization. The methyl group in this compound also makes it an analogue of the six-membered ring molecule methylcyclopropane carboxylate.</p>Formula:C10H17NO4Purity:Min. 95%Molecular weight:215.25 g/mol



