Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H26F3N2O3.Cl |
| Molecular Weight | 422.87 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cl-].[NH3+]CCCC[C@H](NC(=O)C1CCCC1)C(=O)COC2=C(F)C=CC(F)=C2F
InChI
InChIKey=RBFAODLHJICUIM-RSAXXLAASA-N
InChI=1S/C19H25F3N2O3.ClH/c20-13-8-9-14(21)18(17(13)22)27-11-16(25)15(7-3-4-10-23)24-19(26)12-5-1-2-6-12;/h8-9,12,15H,1-7,10-11,23H2,(H,24,26);1H/t15-;/m0./s1
| Molecular Formula | Cl |
| Molecular Weight | 35.453 |
| Charge | -1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C19H26F3N2O3 |
| Molecular Weight | 387.4165 |
| Charge | 1 |
| 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
Sat Dec 16 14:18:29 GMT 2023
by
admin
on
Sat Dec 16 14:18:29 GMT 2023
|
| Record UNII |
7YFE8P1837
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
2211981-77-8
Created by
admin on Sat Dec 16 14:18:29 GMT 2023 , Edited by admin on Sat Dec 16 14:18:29 GMT 2023
|
PRIMARY | |||
|
7YFE8P1837
Created by
admin on Sat Dec 16 14:18:29 GMT 2023 , Edited by admin on Sat Dec 16 14:18:29 GMT 2023
|
PRIMARY | |||
|
300000001946
Created by
admin on Sat Dec 16 14:18:29 GMT 2023 , Edited by admin on Sat Dec 16 14:18:29 GMT 2023
|
PRIMARY | |||
|
153327111
Created by
admin on Sat Dec 16 14:18:29 GMT 2023 , Edited by admin on Sat Dec 16 14:18:29 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |