C₄₉H₄₈BF₂N₅O₁₀

Base Information

Chemical Name:C₄₉H₄₈BF₂N₅O₁₀
CAS No.:1234293-50-5
Molecular Formula:C₄₉H₄₈BF₂N₅O₁₀
Molecular Weight:915.755
Hs Code.:

C<sub>49</sub>H<sub>48</sub>BF<sub>2</sub>N<sub>5</sub>O<sub>10</sub>

Synonyms:C₄₉H₄₈BF₂N₅O₁₀

Suppliers and Price of C₄₉H₄₈BF₂N₅O₁₀

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 C₄₉H₄₈BF₂N₅O₁₀

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₉H₄₈BF₂N₅O₁₀

There total 8 articles about C₄₉H₄₈BF₂N₅O₁₀ 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: 99.0%

: 6066-82-6
1-hydroxy-pyrrolidine-2,5-dione

: 1234293-53-8
C₄₅H₄₅BF₂N₄O₈

: 1234293-50-5
C₄₉H₄₈BF₂N₅O₁₀

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20 ℃; for 16h;
DOI:10.1021/bc100051p

Reference yield:

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

: 1234293-50-5
C₄₉H₄₈BF₂N₅O₁₀

Guidance literature:: Multi-step reaction with 6 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

6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dmap / dichloromethane / 16 h / 0 - 20 °C

With di-isopropyl azodicarboxylate; ammonium acetate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; dmap; 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

: 1234293-50-5
C₄₉H₄₈BF₂N₅O₁₀

Guidance literature:: Multi-step reaction with 4 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

4: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 16 h / 0 - 20 °C

With dmap; di-isopropyl azodicarboxylate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; 1: Mitsunobu reaction;
DOI:10.1021/bc100051p