Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C14H23N |
| Molecular Weight | 205.3391 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCN[C@H](CCC)CC1=CC=CC=C1
InChI
InChIKey=PBENSVGEGPJNFJ-CQSZACIVSA-N
InChI=1S/C14H23N/c1-3-8-14(15-11-4-2)12-13-9-6-5-7-10-13/h5-7,9-10,14-15H,3-4,8,11-12H2,1-2H3/t14-/m1/s1
| Molecular Formula | C14H23N |
| Molecular Weight | 205.3391 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 12:02:19 GMT 2025
by
admin
on
Wed Apr 02 12:02:19 GMT 2025
|
| Record UNII |
UZ3Q3C2Z57
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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784118-64-5
Created by
admin on Wed Apr 02 12:02:19 GMT 2025 , Edited by admin on Wed Apr 02 12:02:19 GMT 2025
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PRIMARY | |||
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159860-08-9
Created by
admin on Wed Apr 02 12:02:19 GMT 2025 , Edited by admin on Wed Apr 02 12:02:19 GMT 2025
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ALTERNATIVE | |||
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Phenylpropylaminopentane
Created by
admin on Wed Apr 02 12:02:19 GMT 2025 , Edited by admin on Wed Apr 02 12:02:19 GMT 2025
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PRIMARY | |||
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UZ3Q3C2Z57
Created by
admin on Wed Apr 02 12:02:19 GMT 2025 , Edited by admin on Wed Apr 02 12:02:19 GMT 2025
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PRIMARY | |||
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DTXSID001296371
Created by
admin on Wed Apr 02 12:02:19 GMT 2025 , Edited by admin on Wed Apr 02 12:02:19 GMT 2025
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PRIMARY | |||
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51529346
Created by
admin on Wed Apr 02 12:02:19 GMT 2025 , Edited by admin on Wed Apr 02 12:02:19 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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RACEMATE -> ENANTIOMER |
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||
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SALT/SOLVATE -> PARENT |
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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