C₃₆H₄₃N₅O₅

Base Information

Chemical Name:C₃₆H₄₃N₅O₅
CAS No.:1429922-23-5
Molecular Formula:C₃₆H₄₃N₅O₅
Molecular Weight:625.768
Hs Code.:

C<sub>36</sub>H<sub>43</sub>N<sub>5</sub>O<sub>5</sub>

Synonyms:

Suppliers and Price of C₃₆H₄₃N₅O₅

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 C₃₆H₄₃N₅O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₆H₄₃N₅O₅

There total 5 articles about C₃₆H₄₃N₅O₅ 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:

: 58196-33-1
7-hydroxy-1,2,3,4-tetrahydroquinoline

: 1429922-23-5
C₃₆H₄₃N₅O₅

: 1429922-24-6
C₃₆H₄₃N₅O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium tetrahydroborate / 2 h / 20 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

2.1: copper(l) iodide; potassium phosphate; 2-Picolinic acid / dimethyl sulfoxide / 85 °C / Sealed tube

3.1: toluene-4-sulfonic acid / 48 h / 20 °C / Inert atmosphere

4.1: sodium iodide; sodium carbonate / acetonitrile / 48 h / Inert atmosphere; Reflux

5.1: hydrogenchloride / water / 0 °C / Inert atmosphere

With 2-Picolinic acid; hydrogenchloride; sodium tetrahydroborate; potassium phosphate; copper(l) iodide; sodium carbonate; toluene-4-sulfonic acid; sodium iodide; In water; dimethyl sulfoxide; acetonitrile;
DOI:10.1002/anie.201205369

Reference yield:

: 22246-18-0
7-hydroxy-3,4-dihydro-2-(1H)-quinolinone

: 1429922-23-5
C₃₆H₄₃N₅O₅

: 1429922-24-6
C₃₆H₄₃N₅O₅

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / Inert atmosphere; Cooling with ice; Reflux

2.1: sodium tetrahydroborate / 2 h / 20 °C / Inert atmosphere

2.2: 20 °C / Inert atmosphere

3.1: copper(l) iodide; potassium phosphate; 2-Picolinic acid / dimethyl sulfoxide / 85 °C / Sealed tube

4.1: toluene-4-sulfonic acid / 48 h / 20 °C / Inert atmosphere

5.1: sodium iodide; sodium carbonate / acetonitrile / 48 h / Inert atmosphere; Reflux

6.1: hydrogenchloride / water / 0 °C / Inert atmosphere

With 2-Picolinic acid; hydrogenchloride; sodium tetrahydroborate; potassium phosphate; copper(l) iodide; lithium aluminium tetrahydride; sodium carbonate; toluene-4-sulfonic acid; sodium iodide; In tetrahydrofuran; water; dimethyl sulfoxide; acetonitrile;
DOI:10.1002/anie.201205369

Reference yield:

: 1429922-14-4
3-(1-ethyl-1,2,3,4-tetrahydroquinolin-7-yloxy)aniline

: 1429922-23-5
C₃₆H₄₃N₅O₅

: 1429922-24-6
C₃₆H₄₃N₅O₅

Guidance literature:: Multi-step reaction with 3 steps

1: toluene-4-sulfonic acid / 48 h / 20 °C / Inert atmosphere

2: sodium iodide; sodium carbonate / acetonitrile / 48 h / Inert atmosphere; Reflux

3: hydrogenchloride / water / 0 °C / Inert atmosphere

With hydrogenchloride; sodium carbonate; toluene-4-sulfonic acid; sodium iodide; In water; acetonitrile;
DOI:10.1002/anie.201205369