C₂₅H₂₄BrNO₈

Base Information

Chemical Name:C₂₅H₂₄BrNO₈
CAS No.:1265221-58-6
Molecular Formula:C₂₅H₂₄BrNO₈
Molecular Weight:546.371
Hs Code.:

C<sub>25</sub>H<sub>24</sub>BrNO<sub>8</sub>

Synonyms:C₂₅H₂₄BrNO₈

Suppliers and Price of C₂₅H₂₄BrNO₈

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 C₂₅H₂₄BrNO₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₅H₂₄BrNO₈

There total 6 articles about C₂₅H₂₄BrNO₈ 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: 62.0%

: 1265221-57-5
C₁₅H₁₂BrNO₆

: 7417-21-2
2-(3,4-dimethoxyphenyl)ethyl alcohol

: 1265221-58-6
C₂₅H₂₄BrNO₈

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; at 18 - 50 ℃; for 15h;
DOI:10.1002/ejoc.201001133

Reference yield:

: 1265221-55-3
C₈H₈INO₄

: 1265221-58-6
C₂₅H₂₄BrNO₈

Guidance literature:: Multi-step reaction with 3 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; tetrabutylammomium bromide; potassium carbonate / tetrahydrofuran; water / 1 h / 60 °C / Inert atmosphere; Microwave irradiation

2: N-Bromosuccinimide / N,N-dimethyl-formamide / 16 h / 18 - 50 °C

3: di-isopropyl azodicarboxylate; triphenylphosphine / 15 h / 18 - 50 °C

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; di-isopropyl azodicarboxylate; tetrabutylammomium bromide; potassium carbonate; triphenylphosphine; In tetrahydrofuran; water; N,N-dimethyl-formamide; 1: Suzuki coupling / 3: Mitsunobu reaction;
DOI:10.1002/ejoc.201001133

Reference yield:

: 1265221-56-4
C₁₅H₁₃NO₆

: 1265221-58-6
C₂₅H₂₄BrNO₈

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide / N,N-dimethyl-formamide / 16 h / 18 - 50 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / 15 h / 18 - 50 °C

With N-Bromosuccinimide; di-isopropyl azodicarboxylate; triphenylphosphine; In N,N-dimethyl-formamide; 2: Mitsunobu reaction;
DOI:10.1002/ejoc.201001133