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CAS 180683-64-1

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(1S,2S)-Boc-1,2-diaminocyclohexane

Description:
(1S,2S)-Boc-1,2-diaminocyclohexane is a chiral organic compound characterized by its bicyclic structure, which includes a cyclohexane ring with two amine functional groups at the 1 and 2 positions. The "Boc" (tert-butyloxycarbonyl) group serves as a protecting group for the amines, enhancing the compound's stability and facilitating its use in various synthetic applications, particularly in peptide synthesis. This compound is typically a white to off-white solid and is soluble in polar organic solvents. Its chirality is significant in pharmaceutical chemistry, as it can influence the biological activity of the resulting compounds. The presence of two amine groups allows for potential interactions in biological systems, making it a valuable intermediate in drug development. Additionally, the compound's stereochemistry can affect its reactivity and interaction with other molecules, which is crucial in designing selective and effective therapeutic agents. Overall, (1S,2S)-Boc-1,2-diaminocyclohexane is an important building block in organic synthesis and medicinal chemistry.
Formula:C11H22N2O2
InChI:InChI=1/C11H22N2O2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8(9)12/h8-9H,4-7,12H2,1-3H3,(H,13,14)/t8-,9-/m0/s1
SMILES:CC(C)(C)OC(=N[C@H]1CCCC[C@@H]1N)O
Synonyms:
  • 1-N-Boc-1(S), 2(S)-Cyclohexyldiamine
  • (1S,2S)-trans-N-Boc-1,2-Cyclohexanediamine
  • 1-N-Boc-(1S,2S)-(+)-1,2-Diaminocyclohexane
  • N-tert-Butoxycarbonyl-S,S-1,2-diaminocyclohexane
  • Carbamic acid, [(1S,2S)-2-aminocyclohexyl]-, 1,1-dimethylethyl ester (9CI)
  • (1S)-trans-N-Boc-1,2-diaminocyclohexane
  • tert-butyl [(1S,2S)-2-aminocyclohexyl]carbamate
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