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N-(1-methylpropyl)-3,4-dimethyl-aniline

Base Information
  • Chemical Name:N-(1-methylpropyl)-3,4-dimethyl-aniline
  • CAS No.:56038-90-5
  • Molecular Formula:C12H19N
  • Molecular Weight:177.29
  • Hs Code.:
  • DSSTox Substance ID:DTXSID101266276
  • Nikkaji Number:J3.166.938C
N-(1-methylpropyl)-3,4-dimethyl-aniline

Synonyms:56038-90-5;N-(1-methylpropyl)-3,4-dimethyl-aniline;N-sec-butyl-3,4-Xylidine;N-butan-2-yl-3,4-dimethylaniline;N-(sec-Butyl)-3,4-dimethylaniline;Benzenamine, 3,4-dimethyl-N-(1-methylpropyl)-;starbld0036670;3,4-Dimethyl-N-(1-methylpropyl)benzenamine;N-(sec-butyl)-3,4-xylidine;SCHEMBL10394672;UYRFXZMCMONWSK-UHFFFAOYSA-N;DTXSID101266276;AKOS000235641

Suppliers and Price of N-(1-methylpropyl)-3,4-dimethyl-aniline
Supply Marketing:
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
  • N-sec-Butyl-3,4-xylidine
  • 250mg
  • $ 275.00
Total 2 raw suppliers
Chemical Property of N-(1-methylpropyl)-3,4-dimethyl-aniline
Chemical Property:
  • XLogP3:4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:177.151749610
  • Heavy Atom Count:13
  • Complexity:144
Purity/Quality:

98% *data from raw suppliers

N-sec-Butyl-3,4-xylidine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC(C)NC1=CC(=C(C=C1)C)C
  • Uses N-sec-Butyl-3,4-xylidine is a useful reagent in the synthesis of dinitro herbicides via one-step dinitration with nitric acid in continuous-flow microreactor.
Technology Process of N-(1-methylpropyl)-3,4-dimethyl-aniline

There total 3 articles about N-(1-methylpropyl)-3,4-dimethyl-aniline 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 naphthalene-2-sulfonate; platinum on carbon; hydrogen; at 60 - 70 ℃; for 1h; under 3750.38 - 7500.75 Torr; Autoclave; Inert atmosphere;
DOI:10.1039/c2gc36652e
Guidance literature:
With potassium amide; for 2h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; Heating;
DOI:10.1021/jo00376a020
Guidance literature:
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