3-Amino-1-hydroxyadamantane
3-Amino-1-hydroxyadamantane structure
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Common Name | 3-Amino-1-hydroxyadamantane | ||
|---|---|---|---|---|
| CAS Number | 702-82-9 | Molecular Weight | 167.248 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 266.8±23.0 °C at 760 mmHg | |
| Molecular Formula | C10H17NO | Melting Point | 265 °C (dec.)(lit.) | |
| MSDS | Chinese USA | Flash Point | 115.2±22.6 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Adamantyl analogues of paracetamol as potent analgesic drugs via inhibition of TRPA1.
PLoS ONE 9(12) , e113841, (2014) Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. We report the synthesis and biological evaluation of adamantyl analogues of paracetamol with important analgesic properties. The mechanism of nociception of compound 6a... |
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Liquid chromatographic methods for the determination of vildagliptin in the presence of its synthetic intermediate and the simultaneous determination of pioglitazone hydrochloride and metformin hydrochloride.
Int. J. Biomed. Sci. 7(3) , 201-8, (2011) Ozone fumigation was explored as a means for degrading organic fungicide residues on fresh produce. Fungicides sorbed onto model abiotic glass surfaces or onto grape berries were fumigated separately in a flow-through chamber. Gaseous ozone at a constant conc... |
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Further calculations on solubility of 3-amino-1-adamantanol in ethanol+ water binary solvent mixtures at various temperatures. Jouyban A, et al.
J. Mol. Liq. 219 , 211-215, (2016)
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A Facile and Economical Method to Synthesize Vildagliptin. Deng Y, et al.
Lett. Org. Chem. 11(10) , 780-784, (2014)
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NOVEL TRICYCLIC CYANOPYRROLIDINE DERIVATIVES AS DPP4 INHIBITORS: AN IMPROVED SYNTHESIS OF TRICYCLIC a-CYCNOPYRROLIDINE FROM CAMPHOR. Arumugam K and Anitha M.
Rasayan J. Chem. 6(3) , 230-237, (2013)
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1-[[(3-hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties.
J. Med. Chem. 46 , 2774-2789, (2003) Dipeptidyl peptidase IV (DPP-IV) inhibition has the potential to become a valuable therapy for type 2 diabetes. The synthesis and structure-activity relationship of a new DPP-IV inhibitor class, N-substituted-glycyl-2-cyanopyrrolidines, are described as well ... |