Details
Stereochemistry | RACEMIC |
Molecular Formula | C15H20Cl2N2O.ClH |
Molecular Weight | 351.699 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(CC(=O)NC1=C(Cl)C=C(Cl)C=C1)N2CCCCC2
InChI
InChIKey=ABPFCLBHEOJRTQ-UHFFFAOYSA-N
InChI=1S/C15H20Cl2N2O.ClH/c1-11(19-7-3-2-4-8-19)9-15(20)18-14-6-5-12(16)10-13(14)17;/h5-6,10-11H,2-4,7-9H2,1H3,(H,18,20);1H
Molecular Formula | C15H20Cl2N2O |
Molecular Weight | 315.238 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://link.springer.com/article/10.1007/BF00771998
Sources: https://link.springer.com/article/10.1007/BF00771998
Clibucaine is a piperidine derivative possessing local anesthetic properties and used in the clinic as a local anesthetic in the 1980s.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:54:36 GMT 2023
by
admin
on
Sat Dec 16 01:54:36 GMT 2023
|
Record UNII |
34D5UD2YMI
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
34D5UD2YMI
Created by
admin on Sat Dec 16 01:54:36 GMT 2023 , Edited by admin on Sat Dec 16 01:54:36 GMT 2023
|
PRIMARY | |||
|
93940-33-1
Created by
admin on Sat Dec 16 01:54:36 GMT 2023 , Edited by admin on Sat Dec 16 01:54:36 GMT 2023
|
PRIMARY | |||
|
300-428-0
Created by
admin on Sat Dec 16 01:54:36 GMT 2023 , Edited by admin on Sat Dec 16 01:54:36 GMT 2023
|
PRIMARY | |||
|
44146892
Created by
admin on Sat Dec 16 01:54:36 GMT 2023 , Edited by admin on Sat Dec 16 01:54:36 GMT 2023
|
PRIMARY | |||
|
DTXSID90917012
Created by
admin on Sat Dec 16 01:54:36 GMT 2023 , Edited by admin on Sat Dec 16 01:54:36 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ENANTIOMER -> RACEMATE | |||
|
ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |