4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

Base Information

Chemical Name:4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate
CAS No.:1451044-05-5
Molecular Formula:C₅₅H₇₉BrO₅
Molecular Weight:900.133
Hs Code.:

Synonyms:4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

Suppliers and Price of 4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

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 4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

There total 6 articles about 4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate 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: 80.0%

: 2536-35-8
16-bromohexadecanoic acid

: 1451044-04-4
4-hydroxyphenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

: 1451044-05-5
4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In tetrahydrofuran; at 50 ℃; for 24h; Inert atmosphere;
DOI:10.1039/c3cc43166e

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1451044-05-5
4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 24 h / 50 °C / Inert atmosphere

2.1: potassium carbonate; 18-crown-6 ether / tetrahydrofuran; dichloromethane / 0.5 h / 20 °C / Inert atmosphere

2.2: 24 h / Reflux

3.1: potassium hydroxide / tetrahydrofuran; ethanol / 12 h / Reflux

3.2: Inert atmosphere

4.1: dmap; triethylamine / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

4.2: 24 h / 55 °C / Inert atmosphere

5.1: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 24 h / 50 °C / Inert atmosphere

With dmap; 18-crown-6 ether; di-isopropyl azodicarboxylate; potassium carbonate; triethylamine; dicyclohexyl-carbodiimide; triphenylphosphine; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1039/c3cc43166e

Reference yield:

: 1451044-01-1
(Z)-4-(octadec-9-en-1-yloxy)benzaldehyde

: 1451044-05-5
4-[(16-bromohexadecanoyl)oxy]phenyl 4-[(E)-2-{4-[(9Z)-octadec-9-en-1-yloxy]phenyl}ethenyl]benzoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate; 18-crown-6 ether / tetrahydrofuran; dichloromethane / 0.5 h / 20 °C / Inert atmosphere

1.2: 24 h / Reflux

2.1: potassium hydroxide / tetrahydrofuran; ethanol / 12 h / Reflux

2.2: Inert atmosphere

3.1: dmap; triethylamine / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

3.2: 24 h / 55 °C / Inert atmosphere

4.1: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 24 h / 50 °C / Inert atmosphere

With dmap; 18-crown-6 ether; potassium carbonate; triethylamine; dicyclohexyl-carbodiimide; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1039/c3cc43166e