CAS 43109-77-9
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9 Produkte.
Adapalene Related Compound C (2-(adamant-1-yl)methoxybenzene)
CAS:Aromatic ethers and their halogenated, sulfonated, nitrated or nitrosated derivativesFormel:C17H22OFarbe und Form:PowderMolekulargewicht:242.167071-(2-Methoxyphenyl)Adamantane
CAS:1-(2-Methoxyphenyl)AdamantaneReinheit:99%Molekulargewicht:242.36g/mol1-(2-Methoxyphenyl)tricyclo[3.3.1.13,7]decane
CAS:Kontrolliertes ProduktFormel:C17H22OFarbe und Form:NeatMolekulargewicht:242.36o-Adamantylanisole
CAS:Kontrolliertes Produkt<p>Impurity Adapalene EP Impurity C<br>Applications An Adamantane anisole derivative used in reaction of adamantane derivatives, including the use of 1-adamantyl, 1-adamantylthio, and 1-adamantylsulfinyl groups as protective groups in amino acid and peptide synthesis. Adapalene EP Impurity C<br>References Saito, S., et al.: Chem. Pharm. Bull., 39, 2718 (1991),<br></p>Formel:C17H22OFarbe und Form:NeatMolekulargewicht:242.36o-Adamantylanisole
CAS:<p>Adamantylanisole is a phenacyl derivative that can be synthesized in two steps. Adamantylanisole is an analog of adamantane that has been functionalized with a phenacyl group, azido group and cyclohexyl group. The adamantanes have been modified to contain fluorides or fluorinated functional groups. Adamantylanisole has shown anti-inflammatory effects in the CNS by inhibiting the synthesis of prostaglandin E2 (PGE2) and nitric oxide (NO). It also has been used as a probe for designing drugs against Alzheimer's disease and Parkinson's disease.</p>Formel:C17H22OReinheit:Min. 95%Molekulargewicht:242.36 g/mol
![1-(2-Methoxyphenyl)tricyclo[3.3.1.13,7]decane](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F86%2Fthumb%2FMM0681.01.jpg&w=3840&q=75)
