| Weight | 139.198 g/mol |
|---|---|
| Formula | C8H13NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Tropinone (532-24-1)
3-tropinone hydrobromide · 3-tropinone · 3-tropinone hydrochloride
Score:
#2250 in Biochemistry
,
#4527 in Biology
,
#5740 in Chemistry
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- Sigma-Aldrich - Search for Tropinone
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- LXIII.A synthesis of tropinone (Journal of The Chemical Society, Transactions, 1917)
- Crystal structures of two tropinone reductases: Different reaction stereospecificities in the same protein fold (Proceedings of the National Academy of Sciences of the United States of America, 1998)
- Two tropinone reductases with different stereospecificities are short-chain dehydrogenases evolved from a common ancestor (Proceedings of the National Academy of Sciences of the United States of America, 1993)
- Two Tropinone Reductases with Distinct Stereospecificities from Cultured Roots of Hyoscyamus niger (Plant Physiology, 1992)
- Two Tropinone Reductases, That Catalyze Opposite Stereospecific Reductions in Tropane Alkaloid Biosynthesis, Are Localized in Plant Root with Different Cell-Specific Patterns (Plant and Cell Physiology, 1999)
- Synthesis of Tropane Alkaloids via Enantioselective Deprotonation of Tropinone (Journal of Organic Chemistry, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-tropinone hydrobromide
- 3-tropinone
- 3-tropinone hydrochloride
-
SMILESCN1C2CCC1CC(=O)C2
-
InChIKeyQQXLDOJGLXJCSE-UHFFFAOYSA-N
- Pubchem - Tropinone
- Wikipedia - Tropinone
Tropinone is an alkaloid, famously synthesised in 1917 by Robert Robinson as a synthetic precursor to atropine, a scarce commodity during World War I. Tropinone and the alkaloids cocaine and atropine all share the same tropane core structure. Its corresponding conjugate acid at pH 7.3 major species is known as tropiniumone.
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