Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C20H32O2 |
| Molecular Weight | 304.4669 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCC(C)(C)C1=CC(O)=C(C=C1)[C@H]2CCC[C@@H](O)C2
InChI
InChIKey=KQUGQXNYBWYGAI-DOTOQJQBSA-N
InChI=1S/C20H32O2/c1-4-5-6-12-20(2,3)16-10-11-18(19(22)14-16)15-8-7-9-17(21)13-15/h10-11,14-15,17,21-22H,4-9,12-13H2,1-3H3/t15-,17+/m0/s1
| Molecular Formula | C20H32O2 |
| Molecular Weight | 304.4669 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:21:34 UTC 2023
by
admin
on
Sat Dec 16 11:21:34 UTC 2023
|
| Record UNII |
DU5BQ63J05
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
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Common Name | English | ||
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Code | English | ||
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Common 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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132296-20-9
Created by
admin on Sat Dec 16 11:21:34 UTC 2023 , Edited by admin on Sat Dec 16 11:21:34 UTC 2023
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PRIMARY | |||
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DU5BQ63J05
Created by
admin on Sat Dec 16 11:21:34 UTC 2023 , Edited by admin on Sat Dec 16 11:21:34 UTC 2023
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PRIMARY | |||
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24041590
Created by
admin on Sat Dec 16 11:21:34 UTC 2023 , Edited by admin on Sat Dec 16 11:21:34 UTC 2023
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PRIMARY | |||
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DTXSID40509880
Created by
admin on Sat Dec 16 11:21:34 UTC 2023 , Edited by admin on Sat Dec 16 11:21:34 UTC 2023
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PRIMARY | |||
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(C6)-CP 47,497
Created by
admin on Sat Dec 16 11:21:34 UTC 2023 , Edited by admin on Sat Dec 16 11:21:34 UTC 2023
|
PRIMARY | (C6)-CP 47,497 (CP 47,497 dimethylhexyl homologue) is a synthetic cannabinoid, a CP 47,497 homologue.Its systematic name is 2-[(1S,3R)-3-hydroxycyclohexyl]-5-(1,1-dimethylhexyl)phenol. |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
