| Weight | 127.187 g/mol |
|---|---|
| Formula | C7H13NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
3-QUINUCLIDINOL (1619-34-7)
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- Discovery of novel quaternary ammonium derivatives of (3R)-quinuclidinol esters as potent and long-acting muscarinic antagonists with potential for minimal systemic exposure after inhaled administration: identification of (3R)-3-{[hydroxy(di-2-thienyl)acetyl]oxy}-1-(3-phenoxypropyl)-1-azoniabicyclo[2.2.2]octane bromide (aclidinium bromide). (Journal of Medicinal Chemistry, 2009)
- Stereoselective synthesis of (R)-3-quinuclidinol through asymmetric reduction of 3-quinuclidinone with 3-quinuclidinone reductase of Rhodotorula rubra (Applied Microbiology and Biotechnology, 2009)
- Enzymatic resolution and cholinergic properties of ()3-quinuclidinol derivatives (Life Sciences, 1977)
- Reaction of geminal diesters with the amine bases 1,5-diazabicyclo[4.3.0]non-5-ene, 1-4-diazabicyclo[2.2.2]octane, and 3-quinuclidinol (Journal of Organic Chemistry, 1976)
- Highly Efficient Synthesis of (R)-3-Quinuclidinol in a SpaceTime Yield of 916 g L1 d1 Using a New Bacterial Reductase ArQR (Organic Letters, 2013)
- A new modified montanari oxidation process by means of chlorine dissolved in the reaction solvent as oxidant and TEMPO as catalyst: Oxidation of 3-S-quinuclidinol to 3-quinuclidinone (Organic Process Research & Development, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CN2CCC1C(C2)O
-
InChIKeyIVLICPVPXWEGCA-UHFFFAOYSA-N
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3-QUINUCLIDINOL
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