C₄₂H₅₀F₃N₅O₁₀S

Base Information

Chemical Name:C₄₂H₅₀F₃N₅O₁₀S
CAS No.:1028252-80-3
Molecular Formula:C₄₂H₅₀F₃N₅O₁₀S
Molecular Weight:873.948
Hs Code.:

C<sub>42</sub>H<sub>50</sub>F<sub>3</sub>N<sub>5</sub>O<sub>10</sub>S

Synonyms:C₄₂H₅₀F₃N₅O₁₀S

Suppliers and Price of C₄₂H₅₀F₃N₅O₁₀S

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 1 raw suppliers

Chemical Property of C₄₂H₅₀F₃N₅O₁₀S

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₂H₅₀F₃N₅O₁₀S

There total 10 articles about C₄₂H₅₀F₃N₅O₁₀S 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: 76.1%

: 1028252-79-0
C₃₁H₃₁F₃N₄O₇S

: 62965-35-9
N-tert-butyloxycarbonyl-L-tert-leucine

: 1028252-80-3
C₄₂H₅₀F₃N₅O₁₀S

Guidance literature:: With 4-methyl-morpholine; HATU; In dichloromethane; at 20 ℃; for 72h;

Reference yield:

: (1S,2R)-1-{[1-Phenyl-meth-(E)-ylidene]-amino}-2-vinyl-cyclopropanecarboxylic acid ethyl ester

: 1028252-80-3
C₄₂H₅₀F₃N₅O₁₀S

Guidance literature:: Multi-step reaction with 9 steps

1.1: hydrogenchloride; water / tert-butyl methyl ether; toluene / 2 h / 20 °C

1.2: 0 °C / pH 14

2.1: tert-butyl methyl ether / 20 °C / Heating / reflux

3.1: sodium hydroxide / savinase 16.0 L / water; dimethyl sulfoxide / 66.66 h / 35 - 48 °C / pH 8.5 - 9 / Resolution of racemate; sodium borate buffer; Enzymatic reaction

4.1: methanol; lithium hydroxide; water / tetrahydrofuran / 20 °C

4.3: pH 4

5.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 0.83 h / Heating / reflux

5.2: 20 h / 20 °C

6.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

7.1: 4-methyl-morpholine; HATU / dichloromethane / 20 °C

8.1: trifluoroacetic acid / dichloromethane; 1,2-dichloro-ethane / 1.5 h / 20 °C

9.1: 4-methyl-morpholine; HATU / dichloromethane / 72 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; methanol; lithium hydroxide; sodium hydroxide; water; HATU; 1,1'-carbonyldiimidazole; trifluoroacetic acid; savinase 16.0 L; In tetrahydrofuran; dichloromethane; tert-butyl methyl ether; water; dimethyl sulfoxide; 1,2-dichloro-ethane; toluene;

Reference yield:

: 213316-32-6,259221-73-3
rac-(1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid ethyl ester

: 1028252-80-3
C₄₂H₅₀F₃N₅O₁₀S

Guidance literature:: Multi-step reaction with 8 steps

1.1: tert-butyl methyl ether / 20 °C / Heating / reflux

2.1: sodium hydroxide / savinase 16.0 L / water; dimethyl sulfoxide / 66.66 h / 35 - 48 °C / pH 8.5 - 9 / Resolution of racemate; sodium borate buffer; Enzymatic reaction

3.1: methanol; lithium hydroxide; water / tetrahydrofuran / 20 °C

3.3: pH 4

4.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 0.83 h / Heating / reflux

4.2: 20 h / 20 °C

5.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

6.1: 4-methyl-morpholine; HATU / dichloromethane / 20 °C

7.1: trifluoroacetic acid / dichloromethane; 1,2-dichloro-ethane / 1.5 h / 20 °C

8.1: 4-methyl-morpholine; HATU / dichloromethane / 72 h / 20 °C

With 4-methyl-morpholine; methanol; lithium hydroxide; sodium hydroxide; water; HATU; 1,1'-carbonyldiimidazole; trifluoroacetic acid; savinase 16.0 L; In tetrahydrofuran; dichloromethane; tert-butyl methyl ether; water; dimethyl sulfoxide; 1,2-dichloro-ethane;