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3,4-Dimethoxynitrobenzene

Base Information Edit
  • Chemical Name:3,4-Dimethoxynitrobenzene
  • CAS No.:709-09-1
  • Molecular Formula:C8H9NO4
  • Molecular Weight:183.164
  • Hs Code.:29093090
  • European Community (EC) Number:211-906-2
  • NSC Number:93382,27974,10116
  • DSSTox Substance ID:DTXSID9061043
  • Nikkaji Number:J150.894F
  • Wikidata:Q63396182
  • Mol file:709-09-1.mol
3,4-Dimethoxynitrobenzene

Synonyms:3,4-Dimethoxynitrobenzene;709-09-1;1,2-Dimethoxy-4-nitrobenzene;4-Nitroveratrole;Benzene, 1,2-dimethoxy-4-nitro-;4-Nitrcveratrole;NSC 27974;3,4-Dimethoxy-1-nitrobenzene;EINECS 211-906-2;NSC 10116;NSC 93382;AI3-20861;Benzene,2-dimethoxy-4-nitro-;3,4-dimethoxylnitrobenzene;4-nitroveratrol;4-Nitro-veratrole;MFCD00007238;4-NITRO-1,2-DIMETHOXYBENZENE;3,4-dimethoxy nitrobenzene;3,4-dimethoxy- nitrobenzene;ghl.PD_Mitscher_leg0.858;SCHEMBL527567;DTXSID9061043;AMY2531;NSC10116;NSC27974;NSC93382;NSC-10116;NSC-27974;NSC-93382;STL388031;AKOS000120729;2-Methoxy-5-nitrophenol, methyl ether;AS-58398;A9319;CS-0127987;D1488;FT-0619307;EN300-18217;D71262;W-104540;Q63396182

Suppliers and Price of 3,4-Dimethoxynitrobenzene
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
  • TRC
  • 4-Nitro-veratrole
  • 10g
  • $ 75.00
  • TRC
  • 4-Nitro-veratrole
  • 5g
  • $ 50.00
  • TCI Chemical
  • 1,2-Dimethoxy-4-nitrobenzene >99.0%(GC)
  • 25g
  • $ 33.00
  • Frontier Specialty Chemicals
  • 4-Nitroveratrole 98%
  • 25g
  • $ 49.00
  • Frontier Specialty Chemicals
  • 4-Nitroveratrole 98%
  • 100g
  • $ 160.00
  • Crysdot
  • 3,4-Dimethoxynitrobenzene 98%
  • 100g
  • $ 114.00
  • American Custom Chemicals Corporation
  • 4-NITRO-VERATROLE 95.00%
  • 5MG
  • $ 502.03
  • Alichem
  • 3,4-Dimethoxynitrobenzene
  • 1g
  • $ 1475.10
  • Alichem
  • 3,4-Dimethoxynitrobenzene
  • 500mg
  • $ 806.85
  • Alichem
  • 3,4-Dimethoxynitrobenzene
  • 250mg
  • $ 494.40
Total 47 raw suppliers
Chemical Property of 3,4-Dimethoxynitrobenzene Edit
Chemical Property:
  • Appearance/Colour:yellow crystals or crystalline powder 
  • Vapor Pressure:1.16E-05mmHg at 25°C 
  • Melting Point:95-98 °C(lit.) 
  • Refractive Index:1.645 
  • Boiling Point:376.9 °C at 760 mmHg 
  • Flash Point:145.9 °C 
  • PSA:64.28000 
  • Density:1.226 g/cm3 
  • LogP:2.13520 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:183.05315777
  • Heavy Atom Count:13
  • Complexity:180
Purity/Quality:

99% *data from raw suppliers

4-Nitro-veratrole *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi,Xn 
  • Hazard Codes:Xn,Xi 
  • Statements: 22-36/37/38 
  • Safety Statements: 36-26 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Nitrogen Compounds -> Nitros, Aromatic
  • Canonical SMILES:COC1=C(C=C(C=C1)[N+](=O)[O-])OC
  • Uses 4-Nitro-veratrole (cas# 709-09-1) is a compound useful in organic synthesis.
Technology Process of 3,4-Dimethoxynitrobenzene

There total 58 articles about 3,4-Dimethoxynitrobenzene 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:
With Nitrogen dioxide; In dichloromethane; in the dark; -78 deg C, 2 min; RT, 15 min;
DOI:10.1016/S0040-4020(01)81329-6
Guidance literature:
With silver carbonate; In dimethyl sulfoxide; at 120 ℃; for 16h;
DOI:10.1039/b916646g
Guidance literature:
With N-Bromosuccinimide; [bis(trifluoroacetoxy)iodo]benzene; sodium nitrite; In acetonitrile; at 20 ℃; for 3h; regioselective reaction;
DOI:10.1039/c5ob00337g
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