CAS 69460-11-3
:(-)-isopinocampheylamine
Description:
(-)-Isopinocampheylamine, with the CAS number 69460-11-3, is an organic compound that belongs to the class of amines. It is a chiral molecule, meaning it has non-superimposable mirror images, which contributes to its unique properties and potential applications in asymmetric synthesis. This compound is derived from isopinocampheol, a bicyclic monoterpene, and is characterized by its amine functional group, which imparts basicity and nucleophilicity. (-)-Isopinocampheylamine is often utilized in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, due to its ability to act as a chiral auxiliary. The compound typically exhibits a solid state at room temperature and may have specific solubility characteristics in organic solvents. Its stereochemistry plays a crucial role in determining its reactivity and interaction with biological systems, making it of interest in medicinal chemistry and drug development. Overall, (-)-isopinocampheylamine is a valuable compound in the field of synthetic organic chemistry.
Formula:C10H19N
InChI:InChI=1/C10H19N/c1-6-8-4-7(5-9(6)11)10(8,2)3/h6-9H,4-5,11H2,1-3H3/t6-,7+,8-,9-/m1/s1
Synonyms:- (1R,2R,3R,5S)-()-Isopinocampheylamine
- (1R,2R,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-amine
- ()-Isopinocampheylamine
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Found 5 products.
(1R,2R,3R,5S)-()-Isopinocampheylamine
CAS:Formula:C10H19NPurity:97%Color and Shape:LiquidMolecular weight:153.2646(1R,2R,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-amine
CAS:(1R,2R,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-aminePurity:98%(1R,2R,3R,5S)-(-)-Isopinocampheylamine
CAS:<p>(1R,2R,3R,5s)-(-)-Isopinocampheylamine (IPCA) is a synthetic sesquiterpene amine that can be synthesized from α-pinene and primary amines. It has been shown to have anti-influenza activity in cell culture models. IPCA showed potent inhibition of influenza A virus replication by inhibiting the viral polymerase. This inhibition was synergistic with amantadine and nitroaldol drugs. The mechanism of action is believed to involve the formation of a stable terpene imine intermediate that reacts with nitrosating agents to form a covalent bond between the amine and the nitro group.</p>Formula:C10H19NPurity:Min. 95%Molecular weight:153.27 g/mol




