2-[4-(1,1-Dimethylethyl)phenoxy]-N-hydroxyacetamide

Base Information

Chemical Name:2-[4-(1,1-Dimethylethyl)phenoxy]-N-hydroxyacetamide
CAS No.:3344-25-0
Molecular Formula:C12H17NO3
Molecular Weight:223.272
Hs Code.:
DSSTox Substance ID:DTXSID001225914
Nikkaji Number:J460.753H

Synonyms:DTXSID001225914;3344-25-0;2-[4-(1,1-Dimethylethyl)phenoxy]-N-hydroxyacetamide

Suppliers and Price of 2-[4-(1,1-Dimethylethyl)phenoxy]-N-hydroxyacetamide

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 4 raw suppliers

Chemical Property of 2-[4-(1,1-Dimethylethyl)phenoxy]-N-hydroxyacetamide

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:223.12084340
Heavy Atom Count:16
Complexity:227

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C1=CC=C(C=C1)OCC(=O)NO

Technology Process of 2-[4-(1,1-Dimethylethyl)phenoxy]-N-hydroxyacetamide

There total 4 articles about 2-[4-(1,1-Dimethylethyl)phenoxy]-N-hydroxyacetamide 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: 97.0%

: 135963-28-9
benzyl (p-tert-butylphenoxy)acetohydroxamate

: 3344-25-0
(p-tert-butylphenoxy)acetohydroxamic acid

Guidance literature:: With hydrogen; palladium; In methanol; acetic acid; at 35 ℃;

Reference yield:

: 1798-04-5
(4-tert-butylphenoxy)acetic acid

: 3344-25-0
(p-tert-butylphenoxy)acetohydroxamic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1) (COCl)2, 2) pyridine / 1) CCl₄, reflux, 2) THF

2: 97 percent / H₂ / Pd / acetic acid; methanol / 35 °C

With pyridine; oxalyl dichloride; hydrogen; palladium; In methanol; acetic acid;

Reference yield:

: 5787-50-8
sodium 4-tert-butylphenolate

: 3344-25-0
4-tert.-Butyl-phenoxy-acethydroxamsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: (i) H₂O, (ii) /BRN= 1718733/, H₂SO₄

2: NH₂OH, NaOMe / methanol

With hydroxylamine; sodium methylate; In methanol;