Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H20O |
| Molecular Weight | 156.2652 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)[C@@H]1CC[C@H](C)C[C@@H]1O
InChI
InChIKey=NOOLISFMXDJSKH-GUBZILKMSA-N
InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9-,10-/m0/s1
| Molecular Formula | C10H20O |
| Molecular Weight | 156.2652 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:45:36 GMT 2025
by
admin
on
Mon Mar 31 23:45:36 GMT 2025
|
| Record UNII |
1JE64OEH7Y
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
3623-53-8
Created by
admin on Mon Mar 31 23:45:36 GMT 2025 , Edited by admin on Mon Mar 31 23:45:36 GMT 2025
|
SUPERSEDED | |||
|
1JE64OEH7Y
Created by
admin on Mon Mar 31 23:45:36 GMT 2025 , Edited by admin on Mon Mar 31 23:45:36 GMT 2025
|
PRIMARY | |||
|
491-02-1
Created by
admin on Mon Mar 31 23:45:36 GMT 2025 , Edited by admin on Mon Mar 31 23:45:36 GMT 2025
|
PRIMARY | |||
|
DTXSID801357335
Created by
admin on Mon Mar 31 23:45:36 GMT 2025 , Edited by admin on Mon Mar 31 23:45:36 GMT 2025
|
PRIMARY | |||
|
207-724-8
Created by
admin on Mon Mar 31 23:45:36 GMT 2025 , Edited by admin on Mon Mar 31 23:45:36 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
RACEMATE -> ENANTIOMER | |||
|
|
RACEMATE -> ENANTIOMER |
