C₂₀H₂₄N₂O₃S

Base Information

Chemical Name:C₂₀H₂₄N₂O₃S
CAS No.:768359-13-3
Molecular Formula:C₂₀H₂₄N₂O₃S
Molecular Weight:372.488
Hs Code.:

C<sub>20</sub>H<sub>24</sub>N<sub>2</sub>O<sub>3</sub>S

Synonyms:

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Chemical Property of C₂₀H₂₄N₂O₃S

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Technology Process of C₂₀H₂₄N₂O₃S

There total 7 articles about C₂₀H₂₄N₂O₃S 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:

: 1878-68-8
2-(4-bromophenyl)-acetic acid

: 768359-13-3
C₂₀H₂₄N₂O₃S

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / water; dichloromethane / 20 °C

2.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / tetrahydrofuran / 20 °C

3.1: diisobutylaluminium hydride / toluene / 4 h / 50 °C

3.2: 24 h / 110 °C

4.1: palladium; formic acid / 24 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; formic acid; diisobutylaluminium hydride; benzotriazol-1-ol; palladium; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; water; toluene;
DOI:10.1016/j.bmcl.2014.06.014

Reference yield:

: 335398-50-0
N-benzyl-2-(4-bromophenyl)-acetamide

: 768359-13-3
C₂₀H₂₄N₂O₃S

Guidance literature:: Multi-step reaction with 3 steps

1.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / tetrahydrofuran / 20 °C

2.1: diisobutylaluminium hydride / toluene / 4 h / 50 °C

2.2: 24 h / 110 °C

3.1: palladium; formic acid / 24 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; formic acid; diisobutylaluminium hydride; palladium; In tetrahydrofuran; toluene;
DOI:10.1016/j.bmcl.2014.06.014

Reference yield:

: 663925-82-4
O-isopropyl 2-tert-butoxy-5-fluorophenylthiocarbamate

: 768359-13-3
C₂₀H₂₄N₂O₃S

Guidance literature:: Multi-step reaction with 5 steps

1.1: tert.-butyl lithium / pentane; tetrahydrofuran / 1.5 h / -70 - -30 °C

1.2: -70 °C

2.1: (1R,2S)-1-Amino-2-indanol; borane / tetrahydrofuran / 0.25 h / 20 °C

3.1: potassium carbonate / acetone; water / 24 h / 50 °C

4.1: diisobutylaluminium hydride / toluene / 4 h / 50 °C

4.2: 24 h / 110 °C

5.1: palladium; formic acid / 24 h / 20 °C

With formic acid; (1R,2S)-1-Amino-2-indanol; borane; tert.-butyl lithium; diisobutylaluminium hydride; potassium carbonate; palladium; In tetrahydrofuran; water; acetone; toluene; pentane; 1.2: |Weinreb Ketone Synthesis / 2.1: |Corey-Bakshi-Shibata Reduction;
DOI:10.1016/j.bmcl.2014.06.014