Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)-

Base Information

Chemical Name:Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)-
CAS No.:105639-05-2
Molecular Formula:C₁₈H₂₃N₃O₃
Molecular Weight:329.399
Hs Code.:
ChEMBL ID:CHEMBL420340
DSSTox Substance ID:DTXSID50147232
Wikidata:Q83012486
Mol file:105639-05-2.mol

Synonyms:105639-05-2;Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)-;5-(4,5-Dihydrooxazol-2-yl)-2-((5-(3-methylisoxazol-5-yl)pentyl)oxy)aniline;Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-[[5-(3-methyl-5-isoxazolyl)pentyl]oxy]-;CHEMBL420340;SCHEMBL9862948;DTXSID50147232;5-(4,5-dihydrooxazol-2-yl)-2-[5-(3-methylisoxazol-5-yl)pentoxy]aniline

Suppliers and Price of Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)-

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 Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)-

Chemical Property:

Vapor Pressure:2.12E-12mmHg at 25°C
Boiling Point:556°C at 760 mmHg
Flash Point:290.1°C
Density:1.25g/cm³
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:8
Exact Mass:329.17394160
Heavy Atom Count:24
Complexity:418

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NOC(=C1)CCCCCOC2=C(C=C(C=C2)C3=NCCO3)N

Technology Process of Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)-

There total 3 articles about Benzenamine, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)- 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: 7.0%

: 98033-85-3
5-(5-bromopentyl)-3-methylisoxazole

: 105639-20-1
2-Amino-4-(4,5-dihydro-oxazol-2-yl)-phenol

: 105639-05-2
5-(4,5-Dihydro-oxazol-2-yl)-2-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-phenylamine

Guidance literature:: With potassium carbonate; sodium iodide; In acetonitrile; for 24h; Heating;
DOI:10.1021/jm00385a021

Reference yield:

: 3-Amino-4-hydroxy-N-(2-hydroxy-ethyl)-benzamide

: 105639-05-2
5-(4,5-Dihydro-oxazol-2-yl)-2-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-phenylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / thionyl chloride / various solvent(s) / 1.5 h / 25 °C

2: 7 percent / NaI, K₂CO₃ / acetonitrile / 24 h / Heating

With thionyl chloride; potassium carbonate; sodium iodide; In acetonitrile;
DOI:10.1021/jm00385a021

Reference yield:

: 13052-92-1
ethyl 3-amino-4-hydroxybenzoate

: 105639-05-2
5-(4,5-Dihydro-oxazol-2-yl)-2-[5-(3-methyl-isoxazol-5-yl)-pentyloxy]-phenylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 2 h / 135 °C

2: 91 percent / thionyl chloride / various solvent(s) / 1.5 h / 25 °C

3: 7 percent / NaI, K₂CO₃ / acetonitrile / 24 h / Heating

With thionyl chloride; potassium carbonate; sodium iodide; In acetonitrile;
DOI:10.1021/jm00385a021