C₄₁H₅₃N₃O₂₃

Base Information

Chemical Name:C₄₁H₅₃N₃O₂₃
CAS No.:96181-94-1
Molecular Formula:C₄₁H₅₃N₃O₂₃
Molecular Weight:955.878
Hs Code.:

C<sub>41</sub>H<sub>53</sub>N<sub>3</sub>O<sub>23</sub>

Synonyms:C₄₁H₅₃N₃O₂₃

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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 C₄₁H₅₃N₃O₂₃

Chemical Property:

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Technology Process of C₄₁H₅₃N₃O₂₃

There total 2 articles about C₄₁H₅₃N₃O₂₃ 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:

: 96181-93-0
C₆₁H₇₁N₃O₂₃

: 96181-94-1
C₄₁H₅₃N₃O₂₃

Guidance literature:: With jones reagent; boron trifluoride diethyl etherate; Multistep reaction; 1.) THF, 2 deg C, 40 min; 2.) r.t., 4 h;
DOI:10.1246/cl.1984.2097

Reference yield:

: 96181-92-9
C₅₉H₆₉N₃O₂₂

: 96181-94-1
C₄₁H₅₃N₃O₂₃

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine

2: 1.) BF₃-Et₂O; 2.) Jones reagent / 1.) THF, 2 deg C, 40 min; 2.) r.t., 4 h

With pyridine; jones reagent; boron trifluoride diethyl etherate;
DOI:10.1246/cl.1984.2097

Reference yield:

: 96181-94-1
C₄₁H₅₃N₃O₂₃

: 25546-65-0
ribostamycin

Guidance literature:: Multi-step reaction with 5 steps

1: benzene; pyridine / 1 h / Heating

2: 62 percent / NaOMe / methanol; nitromethane / 14 h / Ambient temperature

3: 1.) p-TsOH*H₂O; 2.) pyridine; 3.) d-10-camphorsulfonic acid / 1.) DMF, 45 deg C, 50 min; 2.) r.t., 8 h; 3.) DMF, r.t., 10 min

5: 59 percent / 80percent aq. NH₂NH₂*H₂O / 66 h / 100 °C / sealed tube

With pyridine; camphor-10-sulfonic acid; sodium methylate; toluene-4-sulfonic acid; hydrazine hydrate; In pyridine; methanol; nitromethane; benzene;
DOI:10.1246/cl.1984.2097