C₁₉H₂₄N₂O₅S₂Se

Base Information

Chemical Name:C₁₉H₂₄N₂O₅S₂Se
CAS No.:786709-73-7
Molecular Formula:C₁₉H₂₄N₂O₅S₂Se
Molecular Weight:503.502
Hs Code.:

C<sub>19</sub>H<sub>24</sub>N<sub>2</sub>O<sub>5</sub>S<sub>2</sub>Se

Synonyms:

Suppliers and Price of C₁₉H₂₄N₂O₅S₂Se

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 C₁₉H₂₄N₂O₅S₂Se

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₉H₂₄N₂O₅S₂Se

There total 4 articles about C₁₉H₂₄N₂O₅S₂Se 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:

: 1482-82-2
dibenzyl diselenide

: 786709-73-7
C₁₉H₂₄N₂O₅S₂Se

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaBH₄ / ethanol

1.2: 94 percent / ethanol / 1 h

2.1: lithium hexamethyldisilylazide / tetrahydrofuran / 0.17 h / -78 °C

2.2: 92 percent / tetrahydrofuran / -78 - 20 °C

3.1: lithium hexamethyldisilylazide / tetrahydrofuran / 0.17 h / -78 °C

3.2: 80 percent / tetrahydrofuran / 14 h / -78 - 20 °C

4.1: 96 percent / trifluoroacetic acid / CH₂Cl₂ / 2 h / 0 °C

5.1: 70 percent / DCC / CH₂Cl₂ / 3 h / 20 °C

With sodium tetrahydroborate; dicyclohexyl-carbodiimide; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1039/b409242b

Reference yield:

: 359865-70-6
4-[(phenylmethyl)seleno]-2-azetidinone

: 786709-73-7
C₁₉H₂₄N₂O₅S₂Se

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium hexamethyldisilylazide / tetrahydrofuran / 0.17 h / -78 °C

1.2: 92 percent / tetrahydrofuran / -78 - 20 °C

2.1: lithium hexamethyldisilylazide / tetrahydrofuran / 0.17 h / -78 °C

2.2: 80 percent / tetrahydrofuran / 14 h / -78 - 20 °C

3.1: 96 percent / trifluoroacetic acid / CH₂Cl₂ / 2 h / 0 °C

4.1: 70 percent / DCC / CH₂Cl₂ / 3 h / 20 °C

With dicyclohexyl-carbodiimide; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane;
DOI:10.1039/b409242b

Reference yield:

: 359865-71-7
ethyl 2-oxo-4-[(phenylmethyl)seleno]-1-azetidineacetate

: 786709-73-7
C₁₉H₂₄N₂O₅S₂Se

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilylazide / tetrahydrofuran / 0.17 h / -78 °C

1.2: 80 percent / tetrahydrofuran / 14 h / -78 - 20 °C

2.1: 96 percent / trifluoroacetic acid / CH₂Cl₂ / 2 h / 0 °C

3.1: 70 percent / DCC / CH₂Cl₂ / 3 h / 20 °C

With dicyclohexyl-carbodiimide; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane;
DOI:10.1039/b409242b