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2-Amino-4-(benzyloxy)-5-methoxybenzonitrile

Base Information
  • Chemical Name:2-Amino-4-(benzyloxy)-5-methoxybenzonitrile
  • CAS No.:385785-02-4
  • Molecular Formula:C15H14 N2 O2
  • Molecular Weight:254.288
  • Hs Code.:2926909090
  • DSSTox Substance ID:DTXSID90470839
  • Nikkaji Number:J3.633.332D
  • Wikidata:Q82299017
  • Mol file:385785-02-4.mol
2-Amino-4-(benzyloxy)-5-methoxybenzonitrile

Synonyms:2-AMINO-4-(BENZYLOXY)-5-METHOXYBENZONITRILE;385785-02-4;2-amino-5-methoxy-4-phenylmethoxybenzonitrile;Benzonitrile, 2-amino-5-methoxy-4-(phenylmethoxy)-;2-amino-4-benzyloxy-5-methoxybenzonitrile;SCHEMBL3488326;DTXSID90470839;GAOSRWTZALOJOO-UHFFFAOYSA-N;AR2297;MFCD08234438;AKOS015965542;SB81553;2-amino-4benzyloxy-5-methoxybenzonitrile;AS-45318;2-amino-4-benzyloxy-5-methoxy benzonitrile;BB 0256631;CS-0022486;A912917

Suppliers and Price of 2-Amino-4-(benzyloxy)-5-methoxybenzonitrile
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
  • Crysdot
  • 2-Amino-4-(benzyloxy)-5-methoxybenzonitrile 97%
  • 1g
  • $ 545.00
  • Biosynth Carbosynth
  • 2-Amino-4-(Benzyloxy)-5-Methoxybenzonitrile
  • 250 mg
  • $ 275.00
  • Biosynth Carbosynth
  • 2-Amino-4-(Benzyloxy)-5-Methoxybenzonitrile
  • 100 mg
  • $ 219.00
  • Biosynth Carbosynth
  • 2-Amino-4-(Benzyloxy)-5-Methoxybenzonitrile
  • 50 mg
  • $ 137.00
  • Biosynth Carbosynth
  • 2-Amino-4-(Benzyloxy)-5-Methoxybenzonitrile
  • 25 mg
  • $ 70.00
  • Biosynth Carbosynth
  • 2-Amino-4-(Benzyloxy)-5-Methoxybenzonitrile
  • 500 mg
  • $ 440.00
  • American Custom Chemicals Corporation
  • 2-AMINO-4-(BENZYLOXY)-5-METHOXYBENZONITRILE 95.00%
  • 1G
  • $ 1552.32
  • American Custom Chemicals Corporation
  • 2-AMINO-4-(BENZYLOXY)-5-METHOXYBENZONITRILE 95.00%
  • 100MG
  • $ 782.23
  • American Custom Chemicals Corporation
  • 2-AMINO-4-(BENZYLOXY)-5-METHOXYBENZONITRILE 95.00%
  • 5G
  • $ 4669.09
  • AK Scientific
  • 2-Amino-4-(benzyloxy)-5-methoxybenzonitrile
  • 5g
  • $ 1780.00
Total 11 raw suppliers
Chemical Property of 2-Amino-4-(benzyloxy)-5-methoxybenzonitrile
Chemical Property:
  • PSA:68.27000 
  • LogP:3.30928 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:254.105527694
  • Heavy Atom Count:19
  • Complexity:319
Purity/Quality:

97% *data from raw suppliers

2-Amino-4-(benzyloxy)-5-methoxybenzonitrile 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=C(C(=C1)C#N)N)OCC2=CC=CC=C2
Technology Process of 2-Amino-4-(benzyloxy)-5-methoxybenzonitrile

There total 7 articles about 2-Amino-4-(benzyloxy)-5-methoxybenzonitrile 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 sodium dithionite; Na2S2O4; tetrabutyl-ammonium chloride; sodium hydrogencarbonate; In methanol; dichloromethane; water;
Guidance literature:
Multi-step reaction with 2 steps
1: 76 percent / HNO3; AcOH / 20 h / 20 °C
2: 84 percent / aq. Na2S2O4; Bu4NCl / CH2Cl2 / 20 h / 20 °C
With sodium dithionite; tetrabutyl-ammonium chloride; nitric acid; acetic acid; In dichloromethane;
DOI:10.1021/jm050786h
Guidance literature:
Multi-step reaction with 3 steps
1: potassium carbonate / N,N-dimethyl-formamide / 20 °C
2: nitric acid; acetic anhydride / 0 - 20 °C
3: water; iron; ammonium chloride / isopropyl alcohol / Reflux
With water; nitric acid; acetic anhydride; iron; potassium carbonate; ammonium chloride; In N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1021/jm200903z
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