CAS 156047-46-0
:Cyclopropanepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]methylamino]-, (S)-
Description:
Cyclopropanepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]methylamino]-, (S)-, with CAS number 156047-46-0, is a chemical compound characterized by its unique structure that includes a cyclopropane ring and a propanoic acid moiety. This compound features a chiral center, indicated by the (S)- designation, which implies that it exists in a specific stereoisomeric form. The presence of the 1,1-dimethylethoxycarbonyl group contributes to its reactivity and potential applications in organic synthesis. Cyclopropane derivatives are known for their strain due to the angle constraints in the three-membered ring, which can influence their chemical behavior, including reactivity and stability. This compound may exhibit properties typical of amino acids and carboxylic acids, such as solubility in polar solvents and the ability to participate in various chemical reactions, including esterification and amide formation. Its specific applications would depend on its reactivity profile and the functional groups present, making it of interest in medicinal chemistry and synthetic organic chemistry.
Formula:C12H21NO4
InChI:InChI=1S/C12H21NO4/c1-12(2,3)17-11(16)13(4)9(10(14)15)7-8-5-6-8/h8-9H,5-7H2,1-4H3,(H,14,15)/t9-/m0/s1
InChI key:InChIKey=YLAGHBFGSYSQND-VIFPVBQESA-N
SMILES:[C@H](N(C(OC(C)(C)C)=O)C)(CC1CC1)C(O)=O
Synonyms:- Cyclopropanepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]methylamino]-, (S)-
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Found 2 products.
(S)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-cyclopropylpropanoic acid
CAS:Purity:95%Molecular weight:243.3029938
