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489446-72-2

Cyclopentanecarboxylic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (1R,3R)-

Catalog#: AR00ILWW  |   CAS#: 489446-72-2  |   MDL#: MFCD02259729  |   MF: C12H21NO4  |   MW: 243.2994

Packsize Purity Price Availability Quantity
100mg 97% $71.00 Global Stock Buy Now Add To Cart
250mg 97% $170.00 Global Stock Buy Now Add To Cart
500mg 97% $322.00 Global Stock Buy Now Add To Cart
1g 97% $611.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00ILWW
Chemical Name Cyclopentanecarboxylic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (1R,3R)-
CAS Number 489446-72-2
Molecular Formula C12H21NO4
Molecular Weight 243.2994
MDL Number MFCD02259729
SMILES COC(=O)[C@@H]1CC[C@H](C1)NC(=O)OC(C)(C)C

The (1R,3R)-Methyl 3-((tert-butoxycarbonyl)amino)cyclopentanecarboxylate is a versatile compound commonly used in chemical synthesis processes. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique chemical structure and reactivity make it an ideal starting material for the synthesis of complex molecules.In chemical synthesis, this compound is often employed as a chiral building block due to its specific stereochemistry. The (1R,3R) configuration imparts specific spatial arrangements that are crucial for the development of stereochemically pure compounds. By incorporating this compound into a synthetic route, chemists can control the stereochemistry of the final product, leading to higher yields and enhanced selectivity.Additionally, the tert-butoxycarbonyl (Boc) protecting group on the amino moiety provides stability and allows for selective deprotection under mild conditions. This enables chemists to manipulate the molecule at specific sites while protecting other reactive functionalities, facilitating the synthesis of complex molecules with multiple functional groups.Overall, the (1R,3R)-Methyl 3-((tert-butoxycarbonyl)amino)cyclopentanecarboxylate plays a crucial role in chemical synthesis by enabling the construction of intricate structures with precise stereochemical control and functional group manipulation. Its utility in diverse synthetic pathways highlights its significance in the development of novel compounds with potential applications in various industries.
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