2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Base Information

Chemical Name:2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole
CAS No.:1370244-17-9
Molecular Formula:C₂₅H₂₃NO₂S
Molecular Weight:401.529
Hs Code.:

Synonyms:2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Suppliers and Price of 2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

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-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

There total 7 articles about 2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole 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: 56.0%

: 1370244-39-5
2-[2,3-dimethyl-4-(1-oxo-propyl)phenoxy]ethanethioamide

: 613-54-7
2-Bromo-2'-acetonaphthone

: 1370244-17-9
2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Guidance literature:: In methanol; for 24h; Reflux;
DOI:10.1016/j.bmc.2012.02.011

Reference yield:

: 35370-84-4
2-(2,3-dimethylphenoxy)ethanethioamide

: 1370244-17-9
2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: aluminum (III) chloride / carbon disulfide / 4.5 h / 20 - 50 °C

2: methanol / 24 h / Reflux

With aluminum (III) chloride; In methanol; carbon disulfide; 1: Friedel-Crafts acylation;
DOI:10.1016/j.bmc.2012.02.011

Reference yield:

: 35368-58-2
2-(2,3-dimethylphenoxy)acetamide

: 1370244-17-9
2-[2,3-dimethyl-4-(1-oxopropyl)phenoxymethyl]-4-(naphthalen-2-yl)thiazole

Guidance literature:: Multi-step reaction with 3 steps

1: tetraphosphorus decasulfide / tetrahydrofuran / 1.5 h / 50 °C

2: aluminum (III) chloride / carbon disulfide / 4.5 h / 20 - 50 °C

3: methanol / 24 h / Reflux

With aluminum (III) chloride; tetraphosphorus decasulfide; In tetrahydrofuran; methanol; carbon disulfide; 2: Friedel-Crafts acylation;
DOI:10.1016/j.bmc.2012.02.011