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2,4,5-Trimethoxybenzaldehyde

Base Information Edit
  • Chemical Name:2,4,5-Trimethoxybenzaldehyde
  • CAS No.:4460-86-0
  • Deprecated CAS:14374-62-0
  • Molecular Formula:C10H12O4
  • Molecular Weight:196.203
  • Hs Code.:29124990
  • European Community (EC) Number:224-713-3
  • NSC Number:89299
  • UNII:NDU8J2Q00D
  • DSSTox Substance ID:DTXSID1022217
  • Nikkaji Number:J13.494E
  • Wikidata:Q27194435
  • Metabolomics Workbench ID:43958
  • ChEMBL ID:CHEMBL1164301
  • Mol file:4460-86-0.mol
2,4,5-Trimethoxybenzaldehyde

Synonyms:3,4,6-Trimethoxybenzaldehyde;Asaraldehyde;Asaronaldehyde;Asarylaldehyde;Gazarin;NSC 89299;

Suppliers and Price of 2,4,5-Trimethoxybenzaldehyde
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Asarylaldehyde
  • 100mg
  • $ 255.00
  • TRC
  • 2,4,5-Trimethoxybenzaldehyde
  • 10mg
  • $ 45.00
  • TCI Chemical
  • 2,4,5-Trimethoxybenzaldehyde >98.0%(GC)
  • 25g
  • $ 52.00
  • TCI Chemical
  • 2,4,5-Trimethoxybenzaldehyde >98.0%(GC)
  • 5g
  • $ 18.00
  • SynQuest Laboratories
  • 2,4,5-Trimethoxybenzaldehyde 99%
  • 25 g
  • $ 26.00
  • Sigma-Aldrich
  • 2,4,5-Trimethoxybenzaldehyde 98%
  • 25g
  • $ 61.10
  • Sigma-Aldrich
  • 2,4,5-Trimethoxybenzaldehyde 98%
  • 100g
  • $ 160.00
  • Sigma-Aldrich
  • Asarylaldehyde phyproof? Reference Substance
  • 100 mg
  • $ 130.00
  • Matrix Scientific
  • 2,4,5-Trimethoxybenzaldehyde 95%+
  • 1g
  • $ 101.00
  • Matrix Scientific
  • 2,4,5-Trimethoxybenzaldehyde 95%+
  • 5g
  • $ 323.00
Total 152 raw suppliers
Chemical Property of 2,4,5-Trimethoxybenzaldehyde Edit
Chemical Property:
  • Appearance/Colour:white to light beige fine crystalline powder 
  • Vapor Pressure:0.000125mmHg at 25°C 
  • Melting Point:112-114 °C(lit.) 
  • Refractive Index:1.524 
  • Boiling Point:334.7 °C at 760 mmHg 
  • Flash Point:149 °C 
  • PSA:44.76000 
  • Density:1.133 g/cm3 
  • LogP:1.52490 
  • Storage Temp.:2-8°C 
  • Sensitive.:Air Sensitive 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) 
  • Water Solubility.:<0.1 g/100 mL at 22℃ 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:196.07355886
  • Heavy Atom Count:14
  • Complexity:183
Purity/Quality:

99% *data from raw suppliers

Asarylaldehyde *data from reagent suppliers

Safty Information:
  • Pictogram(s): Corrosive
  • Hazard Codes:
  • Statements: 36/37/38-34 
  • Safety Statements: 22-24/25-45-36/37/39-27-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Benzaldehydes
  • Canonical SMILES:COC1=CC(=C(C=C1C=O)OC)OC
  • Uses fly attractant 2,4,5-Trimethoxybenzaldehyde is used in the synthesis of stilbene and hydrostibene derivatives as potential anticancer agents, inhibiting tubulin. Also used in the synthesis of HIV-RT inhibitors. A selective Cox-2 inhibitor.
Technology Process of 2,4,5-Trimethoxybenzaldehyde

There total 44 articles about 2,4,5-Trimethoxybenzaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
difluoromethyl phenyl sulfide; 1,2,4-trimethoxy-benzene; With tin(IV) chloride; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In dichloromethane; water; dimethyl sulfoxide; at 20 ℃; for 2h;
DOI:10.1055/s-0036-1591545
Guidance literature:
With copper(l) iodide; TEMPOL; N,N'-dimethyl-N,N'-bis(2-pyridylmethyl)ethane-1,2-diamine; In acetonitrile; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/S1872-2067(14)60161-3
Guidance literature:
With sodium periodate; osmium(VIII) oxide; N-benzyl-N,N,N-triethylammonium chloride; In tetrahydrofuran; water; microwave irradiation;
DOI:10.1246/cl.2003.780
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