CAS 5511-18-2

Tricyclo[3.3.1.13,7]decane-1-carboxamide

Description:

Tricyclo[3.3.1.1^3,7]decane-1-carboxamide, with the CAS number 5511-18-2, is a bicyclic organic compound characterized by its unique tricyclic structure. This compound features a carboxamide functional group, which contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and materials science. The tricyclic framework provides rigidity and stability, influencing its physical properties such as melting point and solubility. Typically, compounds like this exhibit moderate polarity due to the presence of the amide group, which can engage in hydrogen bonding. The stereochemistry of the tricyclic system may also play a significant role in its biological activity and interactions with other molecules. Overall, tricyclo[3.3.1.1^3,7]decane-1-carboxamide is of interest for its structural complexity and potential utility in synthetic organic chemistry and medicinal applications. Further studies may explore its reactivity, synthesis pathways, and potential uses in drug development or as a building block in organic synthesis.

Formula: C₁₁H₁₇NO

InChI: InChI=1S/C11H17NO/c12-10(13)11-4-7-1-8(5-11)3-9(2-7)6-11/h7-9H,1-6H2,(H2,12,13)

InChI key: InChIKey=CKBZJTAMRPPVSR-UHFFFAOYSA-N

SMILES: C(N)(=O)C12CC3CC(C1)CC(C2)C3

Synonyms:

• 1-Adamantanecarboxamide
• Adamantan-1-carboxamide
• Tricyclo[3.3.1.1^3,7]decane-1-carboxamide
• Tricyclo[3.3.1.13,7]decane-1-carboxamide

Adamantane-1-carboxamide

CAS: 5511-18-2

Formula: C₁₁H₁₇NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 179.2588

Ref: IN-DA003DWW

1-Adamantane carboxamide

CAS: 5511-18-2

1-Adamantane carboxamide is a potent inhibitor of amines and its activity has been tested with a reaction solution. The chemical structure of 1-adamantane carboxamide is shown in Figure 1. This molecule also has inhibitory effects on insulin resistance and nervous system diseases. It was found to have an inhibitory effect on the enzyme DOPA decarboxylase, which is involved in the synthesis of dopamine, norepinephrine and epinephrine. The inhibition of this enzyme leads to increased levels of dopamine in the brain, which can lead to improved cognition, mood and motor skills. 1-Adamantane carboxamide also has a hydroxyl group that mimics the polarizer in biomimetic molecules.

Formula: C₁₁H₁₇NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 179.26 g/mol

Ref: 3D-FA70811

Adamantane-1-carboxamide

CAS: 5511-18-2

Formula: C₁₁H₁₇NO

Purity: 95%

Color and Shape: Solid

Molecular weight: 179.263

Ref: 10-F324780

1-Adamantanecarboxamide-d15

Controlled Product

CAS: 5511-18-2

Applications Reproduction of Sindbis virus strains sensitive and resistant to 1-adamantanecarboxamide.
References Erice, A., et al.: N. Engl. J. Med., 320, 289 (1989), Andronova, V.L., et al.: Bull. Exper. Bio. Med., 129, 74 (2000).

Formula: C₁₁D₁₅H₂NO

Color and Shape: Neat

Molecular weight: 194.351

Ref: TR-A207902

1-Adamantanecarboxamide

Controlled Product

CAS: 5511-18-2

Applications Reproduction of Sindbis virus strains sensitive and resistant to 1-adamantanecarboxamide.
References Erice, A., et al.: N. Engl. J. Med., 320, 289 (1989), Andronova, V.L., et al.: Bull. Exper. Bio. Med., 129, 74 (2000).

Formula: C₁₁H₁₇NO

Color and Shape: Neat

Molecular weight: 179.26

Ref: TR-A207900

1-Adamantanecarboxamide

CAS: 5511-18-2

Formula: C₁₁H₁₇NO

Molecular weight: 179.26

Ref: ST-EA-CP-A73032