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CAS 218772-92-0

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(1R,3R)-3-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid

Description:
(1R,3R)-3-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid is a chiral compound characterized by its cyclohexane ring structure, which features a carboxylic acid functional group and a tert-butoxycarbonyl (Boc) protecting group attached to an amino group. The presence of the Boc group indicates that this compound is likely used in peptide synthesis or as an intermediate in organic synthesis, as it can be easily removed under acidic conditions to reveal the free amine. The specific stereochemistry, denoted by (1R,3R), suggests that the compound has defined spatial arrangements that can influence its reactivity and interactions in biological systems. This compound is typically solid at room temperature and may exhibit solubility in polar organic solvents. Its properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and purity of the sample. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry due to its structural features and potential applications.
Formula:C12H21NO4
InChI:InChI=1/C12H21NO4/c1-12(2,3)17-11(16)13-9-6-4-5-8(7-9)10(14)15/h8-9H,4-7H2,1-3H3,(H,13,16)(H,14,15)/t8-,9-/m1/s1
SMILES:CC(C)(C)OC(=N[C@@H]1CCC[C@H](C1)C(=O)O)O
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