2-Amino-4-butylphenol

Base Information

Chemical Name:2-Amino-4-butylphenol
CAS No.:85533-49-9
Molecular Formula:C10H15NO
Molecular Weight:165.235
Hs Code.:
DSSTox Substance ID:DTXSID80567308
Nikkaji Number:J801.840E
Wikidata:Q82453155

Synonyms:2-amino-4-butylphenol;85533-49-9;p-butyl-aminophenol;SCHEMBL76664;DTXSID80567308;NVKDNDRCUYIBLB-UHFFFAOYSA-N;AKOS017530343

Suppliers and Price of 2-Amino-4-butylphenol

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

Total 0 raw suppliers

Chemical Property of 2-Amino-4-butylphenol

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:165.115364102
Heavy Atom Count:12
Complexity:127

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC1=CC(=C(C=C1)O)N

Technology Process of 2-Amino-4-butylphenol

There total 5 articles about 2-Amino-4-butylphenol 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:

: 52899-59-9
2-nitro-4-butylphenol

: 4'-n-butylbenzoxazinorifamycin

: 85533-49-9
2-amino-4-n-butylphenol

Guidance literature:: With hydrogen; palladium-carbon; In ethanol;

Reference yield:

: 52899-59-9
2-nitro-4-butylphenol

: 85533-49-9
2-amino-4-n-butylphenol

Guidance literature:: With tetrahydrofuran; nickel; Hydrogenation;
DOI:10.1039/jr9550004391

Reference yield:

: 18272-84-9
4-n-butylanisole

: 85533-49-9
2-amino-4-n-butylphenol

Guidance literature:: Multi-step reaction with 3 steps

1: glacial acetic acid; HBr

2: glacial acetic acid; aqueous HNO₃ / 0 - 5 °C

3: alkaline aqueous sodium dithionite

With alkaline aqueous sodium dithionite; hydrogen bromide; nitric acid; acetic acid;