Atomfair 4-Aminoadamantan-1-ol C10H17NO CAS 75375-89-2

4-Aminoadamantan-1-ol (CAS No. 75375-89-2) is a high-purity organic compound with the molecular formula C10H17NO . This derivative of adamantane features both amino and hydroxyl functional groups, making it a valuable intermediate in pharmaceutical and materials science research. Its rigid adamantane backbone provides exceptional thermal and chemical stability, while the functional groups enable further derivatization for drug discovery and polymer applications. Available in >98% purity by HPLC, this compound is supplied as a white to off-white crystalline powder, packaged under inert gas to ensure long-term stability. Ideal for researchers developing novel bioactive molecules or advanced materials.

Description

4-Aminoadamantan-1-ol (CAS No. 75375-89-2) is a high-purity organic compound with the molecular formula C10H17NO. This derivative of adamantane features both amino and hydroxyl functional groups, making it a valuable intermediate in pharmaceutical and materials science research. Its rigid adamantane backbone provides exceptional thermal and chemical stability, while the functional groups enable further derivatization for drug discovery and polymer applications. Available in >98% purity by HPLC, this compound is supplied as a white to off-white crystalline powder, packaged under inert gas to ensure long-term stability. Ideal for researchers developing novel bioactive molecules or advanced materials.

Properties

  • CAS Number: 75375-89-2
  • Complexity: 200
  • IUPAC Name: 4-aminoadamantan-1-ol
  • InChI: InChI=1S/C10H17NO/c11-9-7-1-6-2-8(9)5-10(12,3-6)4-7/h6-9,12H,1-5,11H2
  • InChI Key: HMPCLMSUNVOZLH-UHFFFAOYSA-N
  • Exact Mass: 167.131014166
  • Molecular Formula: C10H17NO
  • Molecular Weight: 167.25
  • SMILES: C1C2CC3CC(C2)(CC1C3N)O
  • Topological: 46.3
  • Monoisotopic Mass: 167.131014166
  • Synonyms: 4-aminoadamantan-1-ol, 75375-89-2, 4-amino-1-adamantanol, 4-amino-1-hydroxyadamantane, Cis-4-aminoadamantan-1-ol, 4-Amino-tricyclo[3.3.1.13,7]decan-1-ol, trans-4-Aminoadamantan-1-ol, 62058-03-1, 62058-13-3, (1r,4s)-4-aminoadamantan-1-ol, (1s,4r)-4-aminoadamantan-1-ol, 5-hydroxytricyclo[3.3.1.13,7 ]decan-2-amine, 1-HYDROXY-4-AMINOADAMANTANE, MFCD12761603, (3S,5S)-4-aminoadamantan-1-ol, MFCD01838554, MFCD16879080, SDCCGMLS-0064885.P001, (1R,3S,4S,5S,7S)-rel-4-Aminoadamantan-1-ol, 4-amino-adamantan-1-ol, 4-amino-adamantane-1-ol, 5-hydroxy-2-adamantanamine, 2-amino-5-hydroxyadamantane, Oprea1_531469, SCHEMBL75490, SCHEMBL256757, SCHEMBL901786, SCHEMBL10138542, SCHEMBL15100743, HMPCLMSUNVOZLH-UHFFFAOYSA-N, ALBB-007397, AC6758, STK387565, AKOS000266030, AKOS016345555, SB84348, CS-12654, SY129243, SY251286, DB-003083, DB-003085, (1s,3r,4r,5s,7s)-4-aminoadamantan-1-ol, 4-aminotricyclo[3.3.1.1~3,7~]decan-1-ol, EN300-146939, EN300-1695480, EN300-6490145, AH-034/11963752

Application

4-Aminoadamantan-1-ol serves as a key building block in medicinal chemistry for the synthesis of antiviral and neurological drugs. Its structural properties make it valuable in developing high-performance polymers with enhanced thermal resistance. Researchers also utilize this compound as a precursor for metal-organic frameworks (MOFs) and other advanced materials.

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