C₄₅H₄₅BF₂N₄O₈

Base Information

Chemical Name:C₄₅H₄₅BF₂N₄O₈
CAS No.:1234293-53-8
Molecular Formula:C₄₅H₄₅BF₂N₄O₈
Molecular Weight:818.682
Hs Code.:

C<sub>45</sub>H<sub>45</sub>BF<sub>2</sub>N<sub>4</sub>O<sub>8</sub>

Synonyms:C₄₅H₄₅BF₂N₄O₈

Suppliers and Price of C₄₅H₄₅BF₂N₄O₈

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 C₄₅H₄₅BF₂N₄O₈

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₅H₄₅BF₂N₄O₈

There total 6 articles about C₄₅H₄₅BF₂N₄O₈ 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: 57.0%

: 108-30-5
succinic acid anhydride

: 1234293-52-7
C₄₆H₄₉BF₂N₄O₇

: 1234293-53-8
C₄₅H₄₅BF₂N₄O₈

Guidance literature:: C₄₆H₄₉BF₂N₄O₇; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;

With sodium hydrogencarbonate; In dichloromethane; water;

succinic acid anhydride; With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 3h;

Reference yield:

: 2657-25-2,38239-52-0,102692-58-0
4'-hydroxychalcone

: 1234293-53-8
C₄₅H₄₅BF₂N₄O₈

Guidance literature:: Multi-step reaction with 5 steps

1.1: diethylamine / ethanol / 16 h / Reflux

2.1: ammonium acetate / ethanol / 24 h / Reflux

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 24 h / 20 °C / Inert atmosphere

4.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 16.33 h / 20 °C

5.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

5.3: 3 h / 20 °C

With di-isopropyl azodicarboxylate; ammonium acetate; diethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane;

Reference yield:

: 1195110-34-9
4,4'-(5,5-difluoro-1,9-diphenyl-5H-4l4,5l4-dipyrrolo[1,2-c:2',1'-f][1,3,5,2]triazaborinine-3,7-diyl)diphenol

: 1234293-53-8
C₄₅H₄₅BF₂N₄O₈

Guidance literature:: Multi-step reaction with 3 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 16 h / 20 °C

2: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3 h / 20 °C

With di-isopropyl azodicarboxylate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; 1: Mitsunobu reaction;
DOI:10.1021/bc100051p