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CAS 35019-66-0

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(4S,5S)-2,2-Dimethyl-4-phenyl-1,3-dioxan-5-amine

Description:
(4S,5S)-2,2-Dimethyl-4-phenyl-1,3-dioxan-5-amine is a chemical compound characterized by its unique structural features, including a dioxane ring and an amine functional group. The presence of two methyl groups at the 2-position and a phenyl group at the 4-position contributes to its steric and electronic properties, which can influence its reactivity and interactions with biological systems. The specific stereochemistry indicated by the (4S,5S) configuration suggests that the compound has distinct spatial arrangements that may affect its pharmacological activity and binding affinity in biological contexts. This compound may be of interest in medicinal chemistry and drug development due to its potential biological activities, although specific applications would depend on further research and characterization. Its CAS number, 35019-66-0, allows for precise identification in chemical databases and literature. Overall, the compound's unique structure and stereochemistry make it a subject of interest for further study in various chemical and pharmaceutical applications.
Formula:C12H17NO2
InChI:InChI=1S/C12H17NO2/c1-12(2)14-8-10(13)11(15-12)9-6-4-3-5-7-9/h3-7,10-11H,8,13H2,1-2H3/t10-,11-/m0/s1
InChI key:InChIKey=ILNGCJMEDIBPTL-QWRGUYRKSA-N
SMILES:N[C@@H]1[C@@H](OC(C)(C)OC1)C2=CC=CC=C2
Synonyms:
  • (4S,5S)-5-Amino-2,2-dimethyl-4-phenyl-1,3-dioxane
  • (4S,5S)-2,2-Dimethyl-4-phenyl-1,3-dioxan-5-amine
  • 1,3-Dioxan-5-amine, 2,2-dimethyl-4-phenyl-, (4S,5S)-
  • L-Acetonamine
  • 1,3-Dioxan-5-amine, 2,2-dimethyl-4-phenyl-, (4S-cis)-
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