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Details

Stereochemistry ACHIRAL
Molecular Formula C9H12O3
Molecular Weight 168.1898
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2,3-TRIMETHOXYBENZENE

SMILES

COC1=CC=CC(OC)=C1OC

InChI

InChIKey=CRUILBNAQILVHZ-UHFFFAOYSA-N
InChI=1S/C9H12O3/c1-10-7-5-4-6-8(11-2)9(7)12-3/h4-6H,1-3H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of cyclophanetetrayne complexes from bis(propargyldicobalt) dication equivalents.
2002 Jul 21
Synthesis and magnetic properties comparison of M-Cu(II) and M-VO(II) Schiff base-porphyrazine complexes: what is the mechanism for spin-coupling?
2005 Jul 13
(Z)-3-(Benzo[b]thiophen-2-yl)-2-(3,4,5-trimethoxyphenyl)acrylonitrile and (E)-3-(benzo[b]thiophen-2-yl)-2-(3,4-dimethoxyphenyl)acrylonitrile. [corrected].
2007 Dec
Luminescence studies of perturbation of tryptophan residues of tubulin in the complexes of tubulin with colchicine and colchicine analogues.
2007 Dec 18
Quantitative 2D HSQC NMR determination of polymer structures by selecting suitable internal standard references.
2007 Jan
The behavior of exciplex decay processes and interplay of radiationless transition and preliminary reorganization mechanisms of electron transfer in loose and tight pairs of reactants.
2007 Jan 18
Identification and characterization of a new tubulin-binding tetrasubstituted brominated pyrrole.
2007 Jul
Arylthioindole inhibitors of tubulin polymerization. 3. Biological evaluation, structure-activity relationships and molecular modeling studies.
2007 Jun 14
Bimolecular hole transfer from the trimethoxybenzene radical cation in the excited state.
2007 Jun 7
Highly efficient ligands for dihydrofolate reductase from Cryptosporidium hominis and Toxoplasma gondii inspired by structural analysis.
2007 Mar 8
(E)-1-(4-Bromo-phen-yl)-3-(3,4,5-trimethoxy-phen-yl)prop-2-en-1-one.
2008 Dec 13
Design, synthesis, and in vitro antitumor activity of new 1,4-diarylimidazole-2-ones and their 2-thione analogues.
2008 Feb 1
3,6-Bis(3,4,5-trimethoxy-phen-yl)-1,2,4-triazolo[3,4-b][1,3,4]thia-diazole.
2008 Jul 23
6-(4-Pyrid-yl)-3-(3,4,5-trimethoxy-phen-yl)-1,2,4-triazolo[3,4-b][1,3,4]thia-diazole.
2008 Jul 31
3,3'-Bis(3,4,5-trimethoxy-benzo-yl)-1,1'-(o-phenyl-ene)dithio-urea ethanol solvate.
2008 Jul 31
Naphthylphenstatins as tubulin ligands: synthesis and biological evaluation.
2008 Oct 1
Ethyl 3-hydr-oxy-13-methyl-4'-phenyl-2'-(3,4,5-trimethoxy-phen-yl)-6,7,8,9,11,12,13,14,15,16-deca-hydro-spiro-[cyclo-penta-[a]phenanthrene-16,3'-pyrrolidine]-5'-carboxyl-ate.
2008 Oct 31
Simultaneous Distillation Extraction of Some Volatile Flavor Components from Pu-erh Tea Samples-Comparison with Steam Distillation-Liquid/Liquid Extraction and Soxhlet Extraction.
2009
3,4,5-Trimeth-oxy-N-(2-methoxy-phen-yl)benzamide.
2009 Jul 22
(E)-1-(2-Thien-yl)-3-(3,4,5-trimethoxy-phen-yl)prop-2-en-1-one.
2009 Jun 13
1-Phenyl-3-(2,4,6-trimethoxy-phen-yl)prop-2-en-1-one.
2009 Oct 23
Synthesis and antimicrobial activity of 3-(1,3,4-Oxadiazol-2-yl)quinazolin-4(3H)-ones.
2010 Apr-Jun
N-(X-Methylphenyl)-2-{(Z)-[(2,3,4-trimethoxyphenyl)methylidene]amino}-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide, where X = 2 and 3.
2010 Dec
Design, synthesis, and biological evaluation of the first podophyllotoxin analogues as potential vascular-disrupting agents.
2010 Dec 3
Patents

Patents

Name Type Language
1,2,3-TRIMETHOXYBENZENE
Systematic Name English
NSC-10124
Code English
PYROGALLOL TRIMETHYL ETHER
Common Name English
Code System Code Type Description
NSC
10124
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
PRIMARY
CAS
634-36-6
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
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PUBCHEM
12462
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
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CHEBI
86529
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
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EPA CompTox
DTXSID1060899
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
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ECHA (EC/EINECS)
211-207-2
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
PRIMARY
FDA UNII
MRE1O894FG
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
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MESH
C091694
Created by admin on Fri Dec 15 18:29:40 GMT 2023 , Edited by admin on Fri Dec 15 18:29:40 GMT 2023
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