Benzenamine, 2-heptyl-4-methoxy-3-methyl-

Base Information

Chemical Name:Benzenamine, 2-heptyl-4-methoxy-3-methyl-
CAS No.:171020-96-5
Molecular Formula:C15H25NO
Molecular Weight:235.37
Hs Code.:
DSSTox Substance ID:DTXSID30455100
Nikkaji Number:J1.819.762F
Wikidata:Q82276962

Synonyms:Benzenamine, 2-heptyl-4-methoxy-3-methyl-;171020-96-5;DTXSID30455100;2-Heptyl-3-methyl-4-methoxyaniline;2-heptyl-4-methoxy-3-methylbenzenamine

Suppliers and Price of Benzenamine, 2-heptyl-4-methoxy-3-methyl-

Supply Marketing:

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

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Chemical Property of Benzenamine, 2-heptyl-4-methoxy-3-methyl-

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:235.193614421
Heavy Atom Count:17
Complexity:195

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC1=C(C=CC(=C1C)OC)N

Technology Process of Benzenamine, 2-heptyl-4-methoxy-3-methyl-

There total 7 articles about Benzenamine, 2-heptyl-4-methoxy-3-methyl- 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: 100.0%

: 1148008-97-2
C₁₅H₁₉NO₃

: 171020-96-5
2-heptyl-4-methoxy-3-methylaniline

Guidance literature:: With palladium 10% on activated carbon; hydrogen; at 20 ℃;
DOI:10.1039/b821039j

Reference yield: 79.0%

: 171020-99-8
3-heptyl-2-methyl-4-nitroanisole

: 171020-96-5
2-heptyl-4-methoxy-3-methylaniline

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 25 ℃; under 800 - 900 Torr;
DOI:10.1016/S0040-4020(02)01180-8

Reference yield:

: 2161-90-2
1-methoxy-1,3-cyclohexadiene

: 171020-96-5
2-heptyl-4-methoxy-3-methylaniline

Guidance literature:: Multi-step reaction with 6 steps

1: 84 percent / 336 h / 200 - 210 °C

2: 100 percent / LiAlH₄ / diethyl ether / 4 h / Heating

3: 93 percent / PBr₃ / diethyl ether / 3 h / Heating

4: 91 percent / LiAlH₄ / diethyl ether / 18 h / Heating

5: 46 percent / HNO₃ / CH₂Cl₂ / 1 h / 25 °C

6: 79 percent / H₂ / 10 percent Pd/C / methanol / 25 °C / 800 - 900 Torr

With lithium aluminium tetrahydride; hydrogen; nitric acid; phosphorus tribromide; palladium on activated charcoal; In methanol; diethyl ether; dichloromethane; 1: Diels-Alder cycloaddition;
DOI:10.1016/S0040-4020(02)01180-8