C₂₉H₃₇FN₄O₂

Base Information

Chemical Name:C₂₉H₃₇FN₄O₂
CAS No.:1350821-90-7
Molecular Formula:C₂₉H₃₇FN₄O₂
Molecular Weight:492.637
Hs Code.:

C<sub>29</sub>H<sub>37</sub>FN<sub>4</sub>O<sub>2</sub>

Synonyms:C₂₉H₃₇FN₄O₂

Suppliers and Price of C₂₉H₃₇FN₄O₂

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 C₂₉H₃₇FN₄O₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₉H₃₇FN₄O₂

There total 7 articles about C₂₉H₃₇FN₄O₂ 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:

: C₄₁H₅₂F₂N₄O₃

: 1350821-90-7
C₂₉H₃₇FN₄O₂

Guidance literature:: With water; sodium hydrogencarbonate; In methanol; at 50 ℃; for 2h;
DOI:10.1016/j.ejmech.2011.06.023

Reference yield:

: 243145-11-1
methyl 3-hydroxymethyltricyclo[3.3.1.1^3,7]decane-1-carboxylate

: 1350821-90-7
C₂₉H₃₇FN₄O₂

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine / dichloromethane / -10 - 20 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride; tert-butyl alcohol / acetonitrile / 1.5 h / 70 °C

3: potassium hydroxide / methanol / Reflux

4: thionyl chloride / acetonitrile / 70 °C / Inert atmosphere

5: triethylamine / acetonitrile / 0.5 h / 20 °C

6: water; sodium hydrogencarbonate / methanol / 2 h / 50 °C

With pyridine; thionyl chloride; tetrabutyl ammonium fluoride; water; sodium hydrogencarbonate; triethylamine; potassium hydroxide; tert-butyl alcohol; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2011.06.023

Reference yield:

: 1350821-96-3
C₁₄H₁₉F₃O₅S

: 1350821-90-7
C₂₉H₃₇FN₄O₂

Guidance literature:: Multi-step reaction with 5 steps

1: tetrabutyl ammonium fluoride; tert-butyl alcohol / acetonitrile / 1.5 h / 70 °C

2: potassium hydroxide / methanol / Reflux

3: thionyl chloride / acetonitrile / 70 °C / Inert atmosphere

4: triethylamine / acetonitrile / 0.5 h / 20 °C

5: water; sodium hydrogencarbonate / methanol / 2 h / 50 °C

With thionyl chloride; tetrabutyl ammonium fluoride; water; sodium hydrogencarbonate; triethylamine; potassium hydroxide; tert-butyl alcohol; In methanol; acetonitrile;
DOI:10.1016/j.ejmech.2011.06.023