Benzenamine, N-butyl-2-methoxy-

Base Information

• Chemical Name: Benzenamine, N-butyl-2-methoxy-
• CAS No.: 65570-20-9
• Molecular Formula: C11H17NO
• Molecular Weight: 179.262
• Hs Code.: 2922299090
• DSSTox Substance ID: DTXSID70215846
• Nikkaji Number: J1.607.758E
• Wikidata: Q83091962
• Mol file: 65570-20-9.mol

Synonyms:n-butyl-2-methoxyaniline;65570-20-9;N-BUTYL-N-(2-METHOXYPHENYL)AMINE;Benzenamine, N-butyl-2-methoxy-;N-Butyl-2-methoxybenzenamine;BRN 3249647;n-butyl-2-anisidine;SCHEMBL6173269;DTXSID70215846;AKOS000231388;LS-28148;EN300-32663

Chemical Property of Benzenamine, N-butyl-2-methoxy-

Chemical Property:

• Vapor Pressure: 0.00983mmHg at 25°C
• Boiling Point: 264.2°C at 760 mmHg
• Flash Point: 107.1°C
• PSA: 21.26000
• Density: 0.982g/cm³
• LogP: 2.98020
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 179.131014166
• Heavy Atom Count: 13
• Complexity: 127

Purity/Quality:

98%min ^*data from raw suppliers

N-Butyl-N-(2-methoxyphenyl)amine ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCNC1=CC=CC=C1OC

Technology Process of Benzenamine, N-butyl-2-methoxy-

There total 20 articles about Benzenamine, N-butyl-2-methoxy- 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%

rac-cysteine (921-01-7,3374-22-9,4371-52-2,40143-64-4,40143-66-6,40143-69-9,52-90-4) + N-butyl-N-(2-methoxyphenyl)-2,4-dinitrobenzenesulfonamide → S-(2,4-Dinitrophenyl)-cystein (3165-76-2) + butyl-(2-methoxy-phenyl)amine (65570-20-9) + sulfur dioxide (7446-09-5,12143-17-8,89125-89-3)

Guidance literature:

In aq. phosphate buffer; for 0.5h; pH=7.4;

DOI:10.1016/j.bmcl.2015.04.046

Reference yield: 100.0%

propyl cyanide (109-74-0) + 2-Nitroanisole (91-23-6) → butyl-(2-methoxy-phenyl)amine (65570-20-9)

Guidance literature:

2-Nitroanisole; With ammonium formate; palladium on activated charcoal; In methanol; water; at 20 ℃;

propyl cyanide; In methanol; water;

DOI:10.1021/ol047580f

Reference yield: 100.0%

propyl cyanide (109-74-0) + 2-methoxy-phenylamine (90-04-0) → butyl-(2-methoxy-phenyl)amine (65570-20-9)

Guidance literature:

With ammonium formate; palladium on activated charcoal; In methanol; water; at 20 ℃; for 3.5h;

DOI:10.1021/ol047580f

upstream raw materials:

1-iodo-butane

2-methoxy-phenylamine

n-Butyl chloride

butan-1-ol

Downstream raw materials:

2-(4-butylamino-3-methoxyphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

2-bromo-N-butyl-N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-methoxyphenyl]-5-methoxybenzamide

N,N-Dibutyl-2-methoxybenzenamine