2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

Base Information

Chemical Name:2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole
CAS No.:1370243-68-7
Molecular Formula:C₂₂H₂₁NO₂S
Molecular Weight:363.48
Hs Code.:

Synonyms:2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

Suppliers and Price of 2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

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-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

There total 10 articles about 2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole 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:

: C₂₄H₂₈N₂O₂S

: 1370243-68-7
2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

Guidance literature:: With sodium hydrogencarbonate; In water; at 85 ℃; for 0.666667h;
DOI:10.1016/j.bmc.2012.02.011

Reference yield:

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

: 1370243-68-7
2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

Guidance literature:: Multi-step reaction with 4 steps

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

2: methanol / 24 h / Reflux

3: acetic acid / 1.5 h / 100 °C

4: sodium hydrogencarbonate / water / 0.67 h / 85 °C

With aluminum (III) chloride; sodium hydrogencarbonate; acetic acid; In methanol; carbon disulfide; water; 1: Friedel-Crafts acylation / 3: Mannich reaction;
DOI:10.1016/j.bmc.2012.02.011

Reference yield:

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

: 1370243-68-7
2-[2,3-dimethyl-4-(2-methylene-1-oxopropyl)phenoxymethyl]-4-phenylthiazole

Guidance literature:: Multi-step reaction with 5 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

4: acetic acid / 1.5 h / 100 °C

5: sodium hydrogencarbonate / water / 0.67 h / 85 °C

With aluminum (III) chloride; tetraphosphorus decasulfide; sodium hydrogencarbonate; acetic acid; In tetrahydrofuran; methanol; carbon disulfide; water; 2: Friedel-Crafts acylation / 4: Mannich reaction;
DOI:10.1016/j.bmc.2012.02.011