Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8ClNO3 |
| Molecular Weight | 201.607 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(C=C(Cl)C(N)=C1)C(O)=O
InChI
InChIKey=RVEATKYEARPWRE-UHFFFAOYSA-N
InChI=1S/C8H8ClNO3/c1-13-7-3-6(10)5(9)2-4(7)8(11)12/h2-3H,10H2,1H3,(H,11,12)
| Molecular Formula | C8H8ClNO3 |
| Molecular Weight | 201.607 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Endogenous 5-HT tonically inhibits spontaneous firing activity of dorsal hippocampus CA1 pyramidal neurons through stimulation of 5-HT(1A) receptors in quiet awake rats: in vivo electrophysiological evidence. | 2001 Feb |
|
| Synthesis and structure-activity relationships of 4-amino-5-chloro-N-(1,4-dialkylhexahydro-1,4-diazepin-6-yl)-2-methoxybenzamide derivatives, novel and potent serotonin 5-HT3 and dopamine D2 receptors dual antagonist. | 2002 Jul |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:10:19 UTC 2023
by
admin
on
Fri Dec 15 19:10:19 UTC 2023
|
| Record UNII |
PQ8L2L84EL
|
| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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7206-70-4
Created by
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PQ8L2L84EL
Created by
admin on Fri Dec 15 19:10:19 UTC 2023 , Edited by admin on Fri Dec 15 19:10:19 UTC 2023
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230-582-3
Created by
admin on Fri Dec 15 19:10:19 UTC 2023 , Edited by admin on Fri Dec 15 19:10:19 UTC 2023
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DTXSID50222391
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admin on Fri Dec 15 19:10:19 UTC 2023 , Edited by admin on Fri Dec 15 19:10:19 UTC 2023
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81626
Created by
admin on Fri Dec 15 19:10:19 UTC 2023 , Edited by admin on Fri Dec 15 19:10:19 UTC 2023
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| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
