C₄₀H₄₄N₄O₅S₃

Base Information Edit

Chemical Name:C₄₀H₄₄N₄O₅S₃
CAS No.:1191242-43-9
Molecular Formula:C₄₀H₄₄N₄O₅S₃
Molecular Weight:757.011
Hs Code.:
Mol file:1191242-43-9.mol

C<sub>40</sub>H<sub>44</sub>N<sub>4</sub>O<sub>5</sub>S<sub>3</sub>

Synonyms:C₄₀H₄₄N₄O₅S₃

Suppliers and Price of C₄₀H₄₄N₄O₅S₃

Supply Marketing:Edit

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 C₄₀H₄₄N₄O₅S₃ Edit

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₀H₄₄N₄O₅S₃

There total 13 articles about C₄₀H₄₄N₄O₅S₃ 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:

: 1092363-38-6
C₅₅H₅₄N₄O₇S₃

: 1191242-43-9
C₄₀H₄₄N₄O₅S₃

Guidance literature:: With diethylamine; In acetonitrile; at 20 ℃; for 5h;
DOI:10.1080/10286020.2010.510114

Reference yield:

: 1092363-40-0
(4R)-methyl 2-(2-((8S)-1-(9H-fluoren-9-yl)-5-isopropyl-3,6,10-trioxo-8-((E)-4-(tritylthio)-but-1-enyl)-2,7-dioxa-4,11-diazadodecan-12-yl)thiazol-4-yl)-4-methyl-4,5-dihydrothiazole-4-carboxylate

: 1191242-43-9
C₄₀H₄₄N₄O₅S₃

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hydroxide / tetrahydrofuran; water / 1.25 h / 0 °C

2: diethylamine / dichloromethane / 3 h / 20 °C

With diethylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jm200432a

Reference yield:

: C₁₀H₁₃N₃O₂S₂*ClH

: 1191242-43-9
C₄₀H₄₄N₄O₅S₃

Guidance literature:: Multi-step reaction with 4 steps

1.1: dmap / dichloromethane / 0.08 h

1.2: 1 h

2.1: dmap; 2,4,6-trichlorobenzoyl chloride; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 0 °C

2.2: 0 - 20 °C

3.1: lithium hydroxide / tetrahydrofuran; water / 1.25 h / 0 °C

4.1: diethylamine / dichloromethane / 3 h / 20 °C

With dmap; 2,4,6-trichlorobenzoyl chloride; diethylamine; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; dichloromethane; water; 2.1: Yamaguchi esterification / 2.2: Yamaguchi esterification;
DOI:10.1021/jm200432a