CAS 2809-78-1
:1-Ethynylcycloheptanol
Description:
1-Ethynylcycloheptanol is an organic compound characterized by its unique structure, which includes a cycloheptane ring and an ethynyl functional group. This compound features a hydroxyl (-OH) group, making it an alcohol, and the presence of the ethynyl group introduces a triple bond, contributing to its reactivity and potential applications in organic synthesis. The molecular formula reflects its composition, which includes carbon, hydrogen, and oxygen atoms. 1-Ethynylcycloheptanol is typically a colorless to pale yellow liquid, exhibiting moderate solubility in organic solvents. Its properties may include a relatively high boiling point due to the presence of the hydroxyl group, which can engage in hydrogen bonding. This compound is of interest in various fields, including medicinal chemistry and materials science, due to its potential as a building block for more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C9H14O
InChI:InChI=1S/C9H14O/c1-2-9(10)7-5-3-4-6-8-9/h1,10H,3-8H2
InChI key:InChIKey=QKJJSXGDSZZUKI-UHFFFAOYSA-N
SMILES:C(#C)C1(O)CCCCCC1
Synonyms:- 1-Ethynyl-1-Cycloheptanol
- Cycloheptanol, 1-Ethynyl-
- NSC 203188
- 1-Ethynylcycloheptanol
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Found 2 products.
1-Ethynylcycloheptan-1-ol
CAS:1-Ethynylcycloheptan-1-ol is a synthetic drug that inhibits protease activity. It has been shown to have an inhibitory effect on the adenosine receptor and protonation of the skeleton. The 1-ethynylcycloheptan-1-ol molecule can be synthesised in two steps from phenylacetone. It has been shown to have hypoglycemic activity, which may be due to its ability to inhibit pancreatic alpha amylase. This drug also has a nucleophilic character, which is essential for its mechanism of action as it binds reversibly to the active site of the enzyme.
Formula:C9H14OPurity:Min. 95%Molecular weight:138.21 g/mol
