Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H23NO2 |
| Molecular Weight | 261.3593 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)O[C@@]1(CCN(C)C[C@H]1C)C2=CC=CC=C2
InChI
InChIKey=UVAZQQHAVMNMHE-CZUORRHYSA-N
InChI=1S/C16H23NO2/c1-4-15(18)19-16(14-8-6-5-7-9-14)10-11-17(3)12-13(16)2/h5-9,13H,4,10-12H2,1-3H3/t13-,16-/m1/s1
| Molecular Formula | C16H23NO2 |
| Molecular Weight | 261.3593 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Three auxiliary medications in obstetrics. 1955]. | 2010-11 |
|
| Structure determination of neoefrapeptins A to N: peptides with insecticidal activity produced by the fungus Geotrichum candidum. | 2006-05 |
|
| Local anesthesia and narcotic drug interaction in pediatric dentistry. | 1988-01-01 |
|
| Ketamine-pancuronium-narcotic technic for cardiovascular surgery in infants--a comparative study. | 1975-11-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:20:47 GMT 2025
by
admin
on
Mon Mar 31 18:20:47 GMT 2025
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| Record UNII |
21J54X4Z4Z
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Official Name | English | ||
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Code | English | ||
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| Classification Tree | Code System | Code | ||
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DEA NO. |
9611
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NCI_THESAURUS |
C1506
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NCI_THESAURUS |
C241
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468-59-7
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CHEMBL14429
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SUB05802MIG
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5284516
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BETAPRODINE
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PRIMARY | |||
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C79779
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21J54X4Z4Z
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DTXSID1046766
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DB01473
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100000085851
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211
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207-411-6
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |