C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

Base Information

Chemical Name:C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S
CAS No.:1443118-38-4
Molecular Formula:C₃₈H₄₆N₂O₁₀S
Molecular Weight:739.722
Hs Code.:

C<sub>38</sub>H<sub>29</sub><sup>(2)</sup>H<sub>17</sub>N<sub>2</sub>O<sub>10</sub>S

Synonyms:C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

Suppliers and Price of C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

Chemical Property:

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

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Technology Process of C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

There total 20 articles about C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S 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: 81.0%

: 4744-10-9
dimethoxypropane

: 1443118-36-2
C₃₅H₂₅⁽²⁾H₁₇N₂O₁₀S

: 1443118-38-4
C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

Guidance literature:: With toluene-4-sulfonic acid; In dichloromethane; water; at 40 ℃; for 1.5h;
DOI:10.1016/j.ejmech.2013.02.001

Reference yield:

: 152438-62-5
(S)-N-[3-Chloro-2-oxo-1-[[4-(phenylmethoxy)phenyl]methyl]propyl]carbamic acid 1,1-dimethylethyl ester

: 1443118-38-4
C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

Guidance literature:: Multi-step reaction with 7 steps

1: sodium borodeuteride / ethanol; tetrahydrofuran / 1 h / -78 - 0 °C

2: potassium hydroxide / ethanol / 1 h / 20 °C

3: tetrahydrofuran / 48 h / 50 °C

4: triethylamine / dichloromethane / 0.83 h / 0 - 20 °C

5: trifluoroacetic acid / dichloromethane / 0.5 h

6: N-ethyl-N,N-diisopropylamine / acetonitrile / 76 °C

7: toluene-4-sulfonic acid / dichloromethane; water / 1.5 h / 40 °C

With sodium borodeuteride; toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1016/j.ejmech.2013.02.001

Reference yield:

: 1256492-59-7
tert-butyl ((2S,3S)-1-(4-(benzyloxy)phenyl)-4-chloro-3-hydroxybutan-2-yl)carbamate-d1

: 1443118-38-4
C₃₈H₂₉⁽²⁾H₁₇N₂O₁₀S

Guidance literature:: Multi-step reaction with 6 steps

1: potassium hydroxide / ethanol / 1 h / 20 °C

2: tetrahydrofuran / 48 h / 50 °C

3: triethylamine / dichloromethane / 0.83 h / 0 - 20 °C

4: trifluoroacetic acid / dichloromethane / 0.5 h

5: N-ethyl-N,N-diisopropylamine / acetonitrile / 76 °C

6: toluene-4-sulfonic acid / dichloromethane; water / 1.5 h / 40 °C

With toluene-4-sulfonic acid; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1016/j.ejmech.2013.02.001