6443-69-2 | 3,4,5-Trimethoxytoluene

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$6.00	$4.00
10g	98%	in stock	$9.00	$6.00
25g	98%	in stock	$15.00	$10.00
100g	97%	in stock	$47.00	$33.00
500g	97%	in stock	$100.00	$70.00

Description

• Catalog Number: AB44306
• Chemical Name: 3,4,5-Trimethoxytoluene
• CAS Number: 6443-69-2
• Molecular Formula: C10H14O3
• Molecular Weight: 182.2164
• MDL Number: MFCD00008397
• SMILES: COc1c(OC)cc(cc1OC)C

Computed Properties

• Complexity: 135
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• XLogP3: 1.8

Literature

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  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120201

• Synthesis and biological evaluation of phenanthrenes as cytotoxic agents with pharmacophore modeling and ChemGPS-NP prediction as topo II inhibitors.

  PloS one 20120101

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  Journal of medicinal chemistry 20100225

• Re-refinement from deposited X-ray data can deliver improved models for most PDB entries.

  Acta crystallographica. Section D, Biological crystallography 20090201

• 1-(4-tert-Butyl-benz-yl)-3-(3,4,5-tri-methoxy-benz-yl)benzimidazolium bromide monohydrate.

  Acta crystallographica. Section E, Structure reports online 20090101

• Constituents of Asarum sieboldii with inhibitory activity on lipopolysaccharide (LPS)-induced NO production in BV-2 microglial cells.

  Chemistry & biodiversity 20080201

• One pot synthesis of alpha-aminophosphonates containing bromo and 3,4,5-trimethoxybenzyl groups under solvent-free conditions.

  Molecules (Basel, Switzerland) 20070207

• Aqueous chlorination of the antibacterial agent trimethoprim: reaction kinetics and pathways.

  Water research 20070201

• Study of the physicochemical properties of trimethoprim with beta-cyclodextrin in solution.

  Journal of pharmaceutical and biomedical analysis 20050615

• New constituents of Leontopodium alpinum and their in vitro leukotriene biosynthesis inhibitory activity.

  Planta medica 20041001

• Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents.

  Journal of medicinal chemistry 20040812

• Synthesis and in vitro platelet aggregation and TP receptor binding studies on bicyclic 5,8-ethanooctahydroisoquinolines and 5,8-ethanotetrahydroisoquinolines.

  Bioorganic & medicinal chemistry 20020801

• QSAR analyses of the substituted indanone and benzylpiperidine rings of a series of indanone-benzylpiperidine inhibitors of acetylcholinesterase.

  Journal of medicinal chemistry 19920207