CAS 16892-50-5
:8-thiabicyclo[3.2.1]octan-3-one
Description:
8-Thiabicyclo[3.2.1]octan-3-one, with the CAS number 16892-50-5, is a bicyclic compound characterized by its unique structure that includes a sulfur atom within a bicyclic framework. This compound features a bicyclo[3.2.1]octane core, which consists of two fused cyclopropane rings, and a ketone functional group at the 3-position. The presence of the sulfur atom contributes to its distinct chemical properties, potentially influencing its reactivity and interactions with other substances. Typically, compounds of this type may exhibit interesting biological activities, making them of interest in medicinal chemistry and synthetic organic chemistry. The compound's physical properties, such as boiling point, melting point, and solubility, can vary based on its molecular structure and functional groups. Additionally, its stereochemistry may play a significant role in its chemical behavior and potential applications. Overall, 8-thiabicyclo[3.2.1]octan-3-one represents a fascinating area of study within the field of organic chemistry.
Formula:C7H10OS
InChI:InChI=1/C7H10OS/c8-5-3-6-1-2-7(4-5)9-6/h6-7H,1-4H2
SMILES:C1CC2CC(=O)CC1S2
Synonyms:- 8-Thiabicyclo[3.2.1]octan-3-one
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
8-Thiabicyclo[3.2.1]octan-3-one
CAS:<p>8-Thiabicyclo[3.2.1]octan-3-one is a chiral tropane alkaloid that is used as an analog for pseudotropine and hyoscyamine. It is metabolized by oxidation, hydroxylation, or amide hydrolysis to form compounds with similar structures to tropane and hyoscyamine. 8-Thiabicyclo[3.2.1]octan-3-one has been shown to inhibit the biosynthesis of dopamine, norepinephrine, and serotonin in rat brain cells; therefore it may have therapeutic potential as a treatment for Parkinson's disease as well as other neurological disorders such as depression and anxiety.</p>Formula:C7H10OSPurity:Min. 95%Molecular weight:142.22 g/mol

