N-[5-Methoxy-2-(1-methylethoxy)phenyl]-3-nitro-2-pyridinamine

Base Information

Chemical Name:N-[5-Methoxy-2-(1-methylethoxy)phenyl]-3-nitro-2-pyridinamine
CAS No.:151598-63-9
Molecular Formula:C₁₅H₁₇N₃O₄
Molecular Weight:303.318
Hs Code.:
DSSTox Substance ID:DTXSID401180451

Synonyms:DTXSID401180451;N-[5-Methoxy-2-(1-methylethoxy)phenyl]-3-nitro-2-pyridinamine;151598-63-9

Suppliers and Price of N-[5-Methoxy-2-(1-methylethoxy)phenyl]-3-nitro-2-pyridinamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[5-Methoxy-2-(1-methylethoxy)phenyl]-3-nitro-2-pyridinamine

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:303.12190603
Heavy Atom Count:22
Complexity:361

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)OC1=C(C=C(C=C1)OC)NC2=C(C=CC=N2)[N+](=O)[O-]

Technology Process of N-[5-Methoxy-2-(1-methylethoxy)phenyl]-3-nitro-2-pyridinamine

There total 3 articles about N-[5-Methoxy-2-(1-methylethoxy)phenyl]-3-nitro-2-pyridinamine 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:

Reference yield: 59.0%

: 5470-18-8,34515-82-7
2-Chloro-3-nitropyridine

: 151598-61-7
2-Isopropoxy-5-methoxyaniline

: 151598-63-9
2-(2-Isopropoxy-5-methoxyanilino)-3-nitropyridine

Guidance literature:: With sodium acetate; acetic acid; Heating;

Reference yield:

: 16169-43-0
4-Isopropoxy-3-nitroanisole

: 151598-63-9
2-(2-Isopropoxy-5-methoxyanilino)-3-nitropyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / H₂ / 10percent Pd/C / methanol / 5 h / 26 °C / 760 Torr

2: 59 percent / NaOAc, gl. AcOH / Heating

With hydrogen; sodium acetate; acetic acid; palladium on activated charcoal; In methanol;

Reference yield:

: 20744-02-9
p-Isopropoxyphenyl methyl ether

: 151598-63-9
2-(2-Isopropoxy-5-methoxyanilino)-3-nitropyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / conc. HNO₃ (d=1.42), propionic acid, gl. AcOH / 0.42 h / 0 °C

2: 94 percent / H₂ / 10percent Pd/C / methanol / 5 h / 26 °C / 760 Torr

3: 59 percent / NaOAc, gl. AcOH / Heating

With hydrogen; nitric acid; sodium acetate; acetic acid; propionic acid; palladium on activated charcoal; In methanol;