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About This Item
Empirical Formula (Hill Notation):
C8H13NO2
CAS Number:
Molecular Weight:
155.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
assay
99%
form
solid
mp
120-121 °C (lit.)
SMILES string
CN1[C@@H]2C[C@H](O)[C@H]1CC(=O)C2
InChI
1S/C8H13NO2/c1-9-5-2-6(10)4-7(9)8(11)3-5/h5,7-8,11H,2-4H2,1H3/t5-,7+,8-/m0/s1
InChI key
UOHSTKWPZWFYTF-ARDNSNSESA-N
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Application
6-Hydroxytropinone was used in the synthesis of N-substituted 6-ethyl or -methyl-8-hydroxy-1,2,3,4,5,6-hexahydro-1,4:2,6-dimethano-3-benzazocines[1].
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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T A Montzka et al.
Journal of medicinal chemistry, 20(3), 453-456 (1977-03-01)
A seres of (+/-)-N-substituted 6-ethyl-or -methyl-8-hydroxy-1,2,3,4,5,6-hexahydro-1,4:2,6-dimethano-3-benzazocines has been prepared from 6 hydroxytropinone. The N-cyclopropylmethyl compounds 10a and 10b were found to be strong narcotic antagonists approximately equivalent to nalorphine. Only slight analgetic activity was found in any of these compounds
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