Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H8NO.Cl |
Molecular Weight | 145.587 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cl-].[NH3+]C1=CC=CC(O)=C1
InChI
InChIKey=DCBCSMXGLXAXDM-UHFFFAOYSA-N
InChI=1S/C6H7NO.ClH/c7-5-2-1-3-6(8)4-5;/h1-4,8H,7H2;1H
Approval Year
PubMed
Title | Date | PubMed |
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Biological monitoring of phenmedipham: determination of m-toluidine in urine. | 2001 May |
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Development and optimization of a reversed-phase high-performance liquid chromatographic method for the determination of acetaminophen and its major metabolites in rabbit plasma and urine after a toxic dose. | 2003 Jul 14 |
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A general and high yielding fragment coupling synthesis of heteroatom-bridged calixarenes and the unprecedented examples of calixarene cavity fine-tuned by bridging heteroatoms. | 2004 Dec 1 |
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Quantitative determination of p-aminosalicylic acid and its degradation product m-aminophenol in pellets by ion-pair high-performance liquid chromatography applying the monolithic Chromolith Speedrod RP-18e column. | 2004 Jan |
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Charge redistribution on electronic excitation. Dipole moments of cis- and trans-3-aminophenol in their S(0) and S(1) electronic states. | 2004 Sep 15 |
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'Green' methodology for efficient and selective benzoylation of nucleosides using benzoyl cyanide in an ionic liquid. | 2005 Jul 15 |
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Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
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Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
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Quinoxaline-3-amino-phenol-water (2/1/2). | 2008 Apr 23 |
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Characterization of an AM404 analogue, N-(3-hydroxyphenyl)arachidonoylamide, as a substrate and inactivator of prostaglandin endoperoxide synthase. | 2009 Dec 29 |
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Prediction of the contact sensitizing potential of chemicals using analysis of gene expression changes in human THP-1 monocytes. | 2010 Nov 10 |
Patents
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Code System | Code | Type | Description | ||
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200-125-2
Created by
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DTXSID10892453
Created by
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51-81-0
Created by
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3045332
Created by
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NQM2XX7XPO
Created by
admin on Sat Dec 16 20:10:26 GMT 2023 , Edited by admin on Sat Dec 16 20:10:26 GMT 2023
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SUBSTANCE RECORD