C₂₉H₃₇F₃N₆O₅

Base Information

Chemical Name:C₂₉H₃₇F₃N₆O₅
CAS No.:618900-60-0
Molecular Formula:C₂₉H₃₇F₃N₆O₅
Molecular Weight:606.645
Hs Code.:

C<sub>29</sub>H<sub>37</sub>F<sub>3</sub>N<sub>6</sub>O<sub>5</sub>

Synonyms:C₂₉H₃₇F₃N₆O₅

Suppliers and Price of C₂₉H₃₇F₃N₆O₅

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 C₂₉H₃₇F₃N₆O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₉H₃₇F₃N₆O₅

There total 7 articles about C₂₉H₃₇F₃N₆O₅ 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: 74.0%

: 416852-11-4
C₁₇H₂₄N₃O₄^(1-)*Li⁽¹⁺⁾

: 618900-59-7
C₁₂H₁₄F₃N₃O₂

: 618900-60-0
C₂₉H₃₇F₃N₆O₅

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; at 70 ℃; for 18h;

Reference yield:

: 695-34-1
2-Amino-4-methylpyridine

: 618900-60-0
C₂₉H₃₇F₃N₆O₅

Guidance literature:: Multi-step reaction with 6 steps

1.1: tert-butyl alcohol / 15 h / 23 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 2.5 h / 23 °C

2.2: 48 h / -78 - 23 °C

3.1: sodium hypochlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate; sodium bromide / dichloromethane; water / 1 h / 0 °C

4.1: acetic acid / dichloromethane / 0.67 h / 23 °C

4.2: 15 h / 23 °C

5.1: lithium hydroxide; water / tetrahydrofuran; methanol / 15 h / 23 °C

6.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane; N,N-dimethyl-formamide / 18 h / 70 °C

With lithium hydroxide; sodium hypochlorite; n-butyllithium; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; water; sodium hydrogencarbonate; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium bromide; In tetrahydrofuran; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 618900-60-0
C₂₉H₃₇F₃N₆O₅

Guidance literature:: Multi-step reaction with 6 steps

1.1: tert-butyl alcohol / 15 h / 23 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 2.5 h / 23 °C

2.2: 48 h / -78 - 23 °C

3.1: sodium hypochlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium hydrogencarbonate; sodium bromide / dichloromethane; water / 1 h / 0 °C

4.1: acetic acid / dichloromethane / 0.67 h / 23 °C

4.2: 15 h / 23 °C

5.1: lithium hydroxide; water / tetrahydrofuran; methanol / 15 h / 23 °C

6.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane; N,N-dimethyl-formamide / 18 h / 70 °C

With lithium hydroxide; sodium hypochlorite; n-butyllithium; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; water; sodium hydrogencarbonate; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium bromide; In tetrahydrofuran; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;