C₂₁H₂₁N₅O₂S

Base Information

Chemical Name:C₂₁H₂₁N₅O₂S
CAS No.:1325216-95-2
Molecular Formula:C₂₁H₂₁N₅O₂S
Molecular Weight:407.496
Hs Code.:

C<sub>21</sub>H<sub>21</sub>N<sub>5</sub>O<sub>2</sub>S

Synonyms:

Suppliers and Price of C₂₁H₂₁N₅O₂S

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 C₂₁H₂₁N₅O₂S

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₁H₂₁N₅O₂S

There total 4 articles about C₂₁H₂₁N₅O₂S 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:

: 1325215-82-4
methyl 2-(5-fluoro-2,4-dinitrophenylamino)acetate

: 1325216-95-2
C₂₁H₂₁N₅O₂S

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 8 h / Reflux

2: palladium 10% on activated carbon; ammonium formate / tetrahydrofuran; ethanol / 3 h / 20 °C

3: acetone / 4 h / Reflux

With palladium 10% on activated carbon; ammonium formate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; acetone;
DOI:10.1021/jm200394x

Reference yield:

: 1325216-71-4
C₁₄H₁₈N₄O₆

: 1325216-95-2
C₂₁H₂₁N₅O₂S

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; ammonium formate / tetrahydrofuran; ethanol / 3 h / 20 °C

2: acetone / 4 h / Reflux

With palladium 10% on activated carbon; ammonium formate; In tetrahydrofuran; ethanol; acetone;
DOI:10.1021/jm200394x

Reference yield:

: 327-92-4
1,5-difluoro-2,4-dinitrobenzene

: 1325216-95-2
C₂₁H₂₁N₅O₂S

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 8 h / Reflux

3: palladium 10% on activated carbon; ammonium formate / tetrahydrofuran; ethanol / 3 h / 20 °C

4: acetone / 4 h / Reflux

With palladium 10% on activated carbon; ammonium formate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; acetone;
DOI:10.1021/jm200394x