C₁₅H₁₉⁽²⁾H₂NO₅S

Base Information

Chemical Name:C₁₅H₁₉⁽²⁾H₂NO₅S
CAS No.:1364077-84-8
Molecular Formula:C₁₅H₂₁NO₅S
Molecular Weight:329.386
Hs Code.:

C<sub>15</sub>H<sub>19</sub><sup>(2)</sup>H<sub>2</sub>NO<sub>5</sub>S

Synonyms:C₁₅H₁₉⁽²⁾H₂NO₅S

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₁₅H₁₉⁽²⁾H₂NO₅S

Chemical Property:

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Technology Process of C₁₅H₁₉⁽²⁾H₂NO₅S

There total 3 articles about C₁₅H₁₉⁽²⁾H₂NO₅S 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:

: 140-88-5,9003-32-1
ethyl acrylate

: 1364077-84-8
C₁₅H₁₉⁽²⁾H₂NO₅S

Guidance literature:: Multi-step reaction with 7 steps

1.1: triethylamine / ethanol / 3.5 h / 35 - 40 °C

2.1: triethylamine / dichloromethane / 4.08 h / 0 - 20 °C

3.1: ethyl [2]alcohol; 1,8-diazabicyclo[5.4.0]undec-7-ene / 94 h / 20 °C / Reflux

4.1: trifluoroacetic acid / dichloromethane / 3.5 h / 0 - 35 °C

4.2: pH 8

5.1: potassium carbonate / acetonitrile / 18.5 h / 5 - 40 °C

6.1: potassium tert-butylate; ethyl [2]alcohol / tetrahydrofuran / 0.78 h / 0 - 5 °C

6.2: 2.25 h / 0 - 5 °C

7.1: triethylamine / dichloromethane / 0.53 h / 0 - 5 °C

With ethyl [2]alcohol; potassium tert-butylate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile;

Reference yield:

: 1364077-75-7
ethyl 3-(benzyl(2-ethoxy-2-oxoethyl)amino)propanoate-d4

: 1364077-84-8
C₁₅H₁₉⁽²⁾H₂NO₅S

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium tert-butylate; ethyl [2]alcohol / tetrahydrofuran / 0.78 h / 0 - 5 °C

1.2: 2.25 h / 0 - 5 °C

2.1: triethylamine / dichloromethane / 0.53 h / 0 - 5 °C

With ethyl [2]alcohol; potassium tert-butylate; triethylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 3783-61-7
diethyl 2-azabutane-1,4-dicarboxylate

: 1364077-84-8
C₁₅H₁₉⁽²⁾H₂NO₅S

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 4.08 h / 0 - 20 °C

2.1: ethyl [2]alcohol; 1,8-diazabicyclo[5.4.0]undec-7-ene / 94 h / 20 °C / Reflux

3.1: trifluoroacetic acid / dichloromethane / 3.5 h / 0 - 35 °C

3.2: pH 8

4.1: potassium carbonate / acetonitrile / 18.5 h / 5 - 40 °C

5.1: potassium tert-butylate; ethyl [2]alcohol / tetrahydrofuran / 0.78 h / 0 - 5 °C

5.2: 2.25 h / 0 - 5 °C

6.1: triethylamine / dichloromethane / 0.53 h / 0 - 5 °C

With ethyl [2]alcohol; potassium tert-butylate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; acetonitrile;