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CAS 177906-48-8

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Trans-N-Boc-1,4-Cyclohexanediamine

Description:
Trans-N-Boc-1,4-cyclohexanediamine is a chemical compound characterized by its bicyclic structure, featuring a cyclohexane ring with two amine functional groups at the 1 and 4 positions. The "N-Boc" designation indicates that one of the amine groups is protected by a tert-butyloxycarbonyl (Boc) group, which is commonly used in organic synthesis to temporarily mask amines and facilitate various reactions. This compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide. It is often utilized in the synthesis of pharmaceuticals and other organic compounds due to its ability to serve as a building block in the formation of more complex structures. The trans configuration of the molecule contributes to its steric and electronic properties, influencing its reactivity and interactions in chemical reactions. As with many amines, it may exhibit basicity and can participate in hydrogen bonding, making it a versatile intermediate in synthetic chemistry.
Formula:C11H22N2O2
InChI:InChI=1/C11H22N2O2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h8-9H,4-7,12H2,1-3H3,(H,13,14)/t8-,9-
SMILES:CC(C)(C)OC(=N[C@H]1CC[C@@H](CC1)N)O
Synonyms:
  • N-Boc-Trans-1,4-Cyclohexanediamine
  • Tert-Butyl Trans-4-Aminocyclohexylcarbamate
  • Trans-(4-Amino-Cyclohexyl)-Carbamic Acid Tert-Butyl Ester
  • Trans-1-Boc-Amino-1,4-Cyclohexanediamine
  • 1-N-Boc-Trans-1,4-Cyclohexyldiamine
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