Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C19H24N2O2 |
Molecular Weight | 312.4061 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]1(C[C@@H]2CC[N@]1C[C@@H]2C=C)[C@@]34NC5=CC=CC=C5[C@]3(O)CCO4
InChI
InChIKey=ALNKTVLUDWIWIH-HLQCWHFUSA-N
InChI=1S/C19H24N2O2/c1-2-13-12-21-9-7-14(13)11-17(21)19-18(22,8-10-23-19)15-5-3-4-6-16(15)20-19/h2-6,13-14,17,20,22H,1,7-12H2/t13-,14-,17-,18+,19-/m0/s1
Molecular Formula | C19H24N2O2 |
Molecular Weight | 312.4061 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Five new alkaloids from the leaves of Remijia peruviana. | 2004 Oct |
|
Ring expansion of sulfur substituted p-quinamines: regiospecific synthesis of 4-aminotropones. | 2005 Feb 28 |
|
Synthesis of 4-aminotropones from [(sulfinyl or sulfonyl)methyl]-substituted p-quinamines. | 2008 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:48:31 GMT 2023
by
admin
on
Sat Dec 16 08:48:31 GMT 2023
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Record UNII |
52XI366326
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Record Status |
Validated (UNII)
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Record Version |
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464-85-7
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207-357-3
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DTXSID10878434
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m448
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admin on Sat Dec 16 08:48:32 GMT 2023 , Edited by admin on Sat Dec 16 08:48:32 GMT 2023
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PRIMARY | Merck Index | ||
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94145
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52XI366326
Created by
admin on Sat Dec 16 08:48:32 GMT 2023 , Edited by admin on Sat Dec 16 08:48:32 GMT 2023
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PRIMARY |
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SALT/SOLVATE -> PARENT |