C₂₄H₂₆ClNO₅

Base Information

Chemical Name:C₂₄H₂₆ClNO₅
CAS No.:1613154-18-9
Molecular Formula:C₂₄H₂₆ClNO₅
Molecular Weight:443.927
Hs Code.:

C<sub>24</sub>H<sub>26</sub>ClNO<sub>5</sub>

Synonyms:C₂₄H₂₆ClNO₅

Suppliers and Price of C₂₄H₂₆ClNO₅

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 C₂₄H₂₆ClNO₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₄H₂₆ClNO₅

There total 7 articles about C₂₄H₂₆ClNO₅ 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: 86.0%

: C₂₄H₂₅BrClNO₅

: 1613154-18-9
C₂₄H₂₆ClNO₅

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; for 2h; Reflux;
DOI:10.1039/c4ob00842a

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 1613154-18-9
C₂₄H₂₆ClNO₅

Guidance literature:: Multi-step reaction with 6 steps

1: tetra-(n-butyl)ammonium iodide; potassium carbonate / N,N-dimethyl-formamide / 20 °C

2: sodium hydroxide / ethanol / 3 h / Reflux

3: diphenyl phosphoryl azide; N-ethyl-N,N-diisopropylamine / Reflux

4: N-Bromosuccinimide; dmap / tetrahydrofuran; methanol / 1 h / 0 °C

5: sodium hydride; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 20 °C

6: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 2 h / Reflux

With dmap; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); diphenyl phosphoryl azide; tri-n-butyl-tin hydride; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; toluene; 3: |Curtius Rearrangement;
DOI:10.1039/c4ob00842a

Reference yield:

: 1613154-12-3
C₁₉H₁₈O₅

: 1613154-18-9
C₂₄H₂₆ClNO₅

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydroxide / ethanol / 3 h / Reflux

2: diphenyl phosphoryl azide; N-ethyl-N,N-diisopropylamine / Reflux

3: N-Bromosuccinimide; dmap / tetrahydrofuran; methanol / 1 h / 0 °C

4: sodium hydride; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 20 °C

5: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 2 h / Reflux

With dmap; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); diphenyl phosphoryl azide; tri-n-butyl-tin hydride; tetra-(n-butyl)ammonium iodide; sodium hydride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; toluene; 2: |Curtius Rearrangement;
DOI:10.1039/c4ob00842a