C₃₀H₄₀N₂O₈S₂

Base Information

Chemical Name:C₃₀H₄₀N₂O₈S₂
CAS No.:156143-73-6
Molecular Formula:C₃₀H₄₀N₂O₈S₂
Molecular Weight:620.788
Hs Code.:

C<sub>30</sub>H<sub>40</sub>N<sub>2</sub>O<sub>8</sub>S<sub>2</sub>

Synonyms:C₃₀H₄₀N₂O₈S₂

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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 C₃₀H₄₀N₂O₈S₂

Chemical Property:

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Technology Process of C₃₀H₄₀N₂O₈S₂

There total 7 articles about C₃₀H₄₀N₂O₈S₂ 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:

: 52117-00-7
2-Acetylamino-2-[(3-cyanophenyl)-methyl]-malonic acid diethyl ester

: 156143-73-6
C₃₀H₄₀N₂O₈S₂

Guidance literature:: Multi-step reaction with 6 steps

1: 100 percent / 6 N aq. HCl / 130 °C

2: 90 percent / SOCl₂

3: 79 percent / dimethylformamide

4: 48 percent / NaBH₄ / ethanol; H₂O / 4 h / 50 °C

5: 56 percent / PPh₃, diisopropyl azodicarboxylate / tetrahydrofuran / Ambient temperature

6: 1.) 1 N NaOH, 2.) I₂ / 1.) EtOH, a) 0 deg C, 30 min, b) RT, 3 h, 2.) EtOH

With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; thionyl chloride; di-isopropyl azodicarboxylate; iodine; triphenylphosphine; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00035a014

Reference yield:

: 80852-34-2
3-Carboxyphenylalanin-hydrochlorid

: 156143-73-6
C₃₀H₄₀N₂O₈S₂

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / SOCl₂

2: 79 percent / dimethylformamide

3: 48 percent / NaBH₄ / ethanol; H₂O / 4 h / 50 °C

4: 56 percent / PPh₃, diisopropyl azodicarboxylate / tetrahydrofuran / Ambient temperature

5: 1.) 1 N NaOH, 2.) I₂ / 1.) EtOH, a) 0 deg C, 30 min, b) RT, 3 h, 2.) EtOH

With sodium hydroxide; sodium tetrahydroborate; thionyl chloride; di-isopropyl azodicarboxylate; iodine; triphenylphosphine; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00035a014

Reference yield:

: 156143-71-4
3-(2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-benzoic acid methyl ester

: 156143-73-6
C₃₀H₄₀N₂O₈S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / PPh₃, diisopropyl azodicarboxylate / tetrahydrofuran / Ambient temperature

2: 1.) 1 N NaOH, 2.) I₂ / 1.) EtOH, a) 0 deg C, 30 min, b) RT, 3 h, 2.) EtOH

With sodium hydroxide; di-isopropyl azodicarboxylate; iodine; triphenylphosphine; In tetrahydrofuran;
DOI:10.1021/jm00035a014