C₃₁H₄₄BrN₅O₂Si

Base Information

Chemical Name:C₃₁H₄₄BrN₅O₂Si
CAS No.:1276126-19-2
Molecular Formula:C₃₁H₄₄BrN₅O₂Si
Molecular Weight:626.712
Hs Code.:

C<sub>31</sub>H<sub>44</sub>BrN<sub>5</sub>O<sub>2</sub>Si

Synonyms:C₃₁H₄₄BrN₅O₂Si

Suppliers and Price of C₃₁H₄₄BrN₅O₂Si

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 C₃₁H₄₄BrN₅O₂Si

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₁H₄₄BrN₅O₂Si

There total 12 articles about C₃₁H₄₄BrN₅O₂Si 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: 76.0%

: 1276125-34-8
C₁₁H₂₂N₄OSi

: 1276126-18-1
C₂₀H₂₄BrNO₂

: 1276126-19-2
C₃₁H₄₄BrN₅O₂Si

Guidance literature:: C₂₀H₂₄BrNO₂; With N-ethyl-N,N-diisopropylamine; HATU; In dichloromethane; at 0 ℃; for 0.5h;

C₁₁H₂₂N₄OSi; In dichloromethane; at 10 ℃; for 24h; Reflux;

Reference yield:

: 1276125-31-5
3-Amino-4,6-dihydro-1H-pyrrolo[3,4-c]pyrazole-5-carboxylic acid benzyl ester

: 1276126-19-2
C₃₁H₄₄BrN₅O₂Si

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.33 h / 0 °C

1.2: 20 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 6 h / 20 °C / 760.05 Torr

3.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 0.5 h / 0 °C

3.2: 24 h / 10 °C / Reflux

With hydrogen; sodium hydride; N-ethyl-N,N-diisopropylamine; HATU; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; mineral oil;

Reference yield:

: 44981-94-4
N-cyanoethyl glycine ethyl ester

: 1276126-19-2
C₃₁H₄₄BrN₅O₂Si

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 3 h / Inert atmosphere; Cooling with ice bath

2.1: sodium hydride / tetrahydrofuran / 20 °C / Inert atmosphere

2.2: pH 3 / Ice water

3.1: hydrazine dihydrochloride / ethanol / 2.5 h / 60 °C

4.1: sodium hydride / tetrahydrofuran; mineral oil / 0.33 h / 0 °C

4.2: 20 °C

5.1: hydrogen / palladium 10% on activated carbon / ethanol / 6 h / 20 °C / 760.05 Torr

6.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 0.5 h / 0 °C

6.2: 24 h / 10 °C / Reflux

With hydrazine dihydrochloride; hydrogen; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; mineral oil;