C₃₅H₄₃N₅O₅

Base Information

Chemical Name:C₃₅H₄₃N₅O₅
CAS No.:1673535-02-8
Molecular Formula:C₃₅H₄₃N₅O₅
Molecular Weight:613.757
Hs Code.:

C<sub>35</sub>H<sub>43</sub>N<sub>5</sub>O<sub>5</sub>

Synonyms:

Suppliers and Price of C₃₅H₄₃N₅O₅

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
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price

Total 3 raw suppliers

Chemical Property of C₃₅H₄₃N₅O₅

Chemical Property:

Purity/Quality:: 98% ,99% , ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₅H₄₃N₅O₅

There total 8 articles about C₃₅H₄₃N₅O₅ 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: 90.0%

: C₅₀H₅₃N₅O₇

: 1673535-02-8
C₃₅H₄₃N₅O₅

Guidance literature:: With diethylamine; In dichloromethane; at 20 ℃; for 0.5h;

Reference yield:

: 13734-38-8,20887-86-9
N-(t-butyloxycarbonyl)-O-(t-butyl)-L-Serine

: 1673535-02-8
C₃₅H₄₃N₅O₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: chloroformic acid ethyl ester; 4-methyl-morpholine / tetrahydrofuran / 0.33 h / -20 °C

1.2: 0.33 h / 0 - 5 °C

2.1: trifluoroacetic anhydride; pyridine / 3 h / 20 °C

3.1: hydroxylamine hydrochloride; potassium carbonate / ethanol / 2 h / 90 °C

4.1: (bis-(2-methoxyethyl)amino)sulfur trufluoride / dichloromethane / 3 h / 0 °C

4.2: 12 h / 20 °C

4.3: 2 h / 90 °C

5.1: diethylamine / dichloromethane / 0.5 h / 20 °C

With 4-methyl-morpholine; pyridine; hydroxylamine hydrochloride; chloroformic acid ethyl ester; potassium carbonate; diethylamine; trifluoroacetic anhydride; (bis-(2-methoxyethyl)amino)sulfur trufluoride; In tetrahydrofuran; ethanol; dichloromethane;

Reference yield:

: C₁₂H₂₄N₂O₄

: 1673535-02-8
C₃₅H₄₃N₅O₅

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluoroacetic anhydride; pyridine / 3 h / 20 °C

2.1: hydroxylamine hydrochloride; potassium carbonate / ethanol / 2 h / 90 °C

3.1: (bis-(2-methoxyethyl)amino)sulfur trufluoride / dichloromethane / 3 h / 0 °C

3.2: 12 h / 20 °C

3.3: 2 h / 90 °C

4.1: diethylamine / dichloromethane / 0.5 h / 20 °C

With pyridine; hydroxylamine hydrochloride; potassium carbonate; diethylamine; trifluoroacetic anhydride; (bis-(2-methoxyethyl)amino)sulfur trufluoride; In ethanol; dichloromethane;