Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H5ClO3 |
| Molecular Weight | 172.566 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC(Cl)=CC=C1O
InChI
InChIKey=NKBASRXWGAGQDP-UHFFFAOYSA-N
InChI=1S/C7H5ClO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Anaerobic degradation and dehalogenation of chlorosalicylates and salicylate under four reducing conditions. | 2001 |
|
| Salicylate activity. 3. Structure relationship to systemic acquired resistance. | 2005 Dec 14 |
|
| Salicylate activity. 1. Protection of plants from paraquat injury. | 2005 Dec 14 |
|
| Guest-controlling effects on ER behaviors of beta-cyclodextrin polymer. | 2005 Sep 1 |
|
| Bis(5-chloro-salicylato-κO)bis-(1,10-phenanthroline-κN,N')cadmium(II). | 2008 Jun 7 |
|
| trans-Dienelactone hydrolase from Pseudomonas reinekei MT1, a novel zinc-dependent hydrolase. | 2008 Nov 14 |
|
| Transport evaluation of salicylic acid and structurally related compounds across Caco-2 cell monolayers and artificial PAMPA membranes. | 2008 Oct |
|
| In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II. | 2008 Oct 15 |
|
| Novel metal-binding site of Pseudomonas reinekei MT1 trans-dienelactone hydrolase. | 2009 Dec 25 |
|
| Deciphering the photophysics of 5-chlorosalicylic acid: evidence for excited-state intramolecular proton transfer. | 2010 Jan |
|
| catena-Poly[[(1,10-phenanthroline)lead(II)]bis-(μ-5-chloro-2-hy-droxy-benzoato)]. | 2010 Jul 21 |
|
| Bismuth(III) complexes derived from non-steroidal anti-inflammatory drugs and their activity against Helicobacter pylori. | 2010 Mar 21 |
|
| SA-ABA antagonism in defense responses. | 2010 Oct |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
206-283-9
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
J2YFG68VCZ
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
9447
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
321-14-2
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
DTXSID7059806
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
100000143079
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
SUB118438
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
30111
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
420128
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY | |||
|
C015751
Created by
admin on Fri Dec 15 19:11:56 GMT 2023 , Edited by admin on Fri Dec 15 19:11:56 GMT 2023
|
PRIMARY |
PARENT (METABOLITE)
PARENT (METABOLITE)
SUBSTANCE RECORD
