C₃₄H₄₁Cl₂N₃O₉S

Base Information

Chemical Name:C₃₄H₄₁Cl₂N₃O₉S
CAS No.:1610859-90-9
Molecular Formula:C₃₄H₄₁Cl₂N₃O₉S
Molecular Weight:738.686
Hs Code.:

C<sub>34</sub>H<sub>41</sub>Cl<sub>2</sub>N<sub>3</sub>O<sub>9</sub>S

Synonyms:C₃₄H₄₁Cl₂N₃O₉S

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Chemical Property of C₃₄H₄₁Cl₂N₃O₉S

Chemical Property:

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Technology Process of C₃₄H₄₁Cl₂N₃O₉S

There total 9 articles about C₃₄H₄₁Cl₂N₃O₉S 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:

: 7357-67-7
4-(3-chloropropyl)morpholine

: 1610859-89-6
(S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(methylsulfonamido)benzoyloxy)-2-(3,4-dimethoxyphenyl)ethyl)pyridine 1-oxide

: 1610859-90-9
C₃₄H₄₁Cl₂N₃O₉S

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 45 ℃;

Reference yield:

: 100868-46-0
3,5-dichloro-4-picoline

: 1610859-90-9
C₃₄H₄₁Cl₂N₃O₉S

Guidance literature:: Multi-step reaction with 8 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

1.2: -78 - 20 °C

2.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 2 h / 20 °C

3.1: methanol; chloroform / 2 h / 20 °C

4.1: potassium tert-butylate; methanol / toluene / 24 h / 20 °C

5.1: 3-chloro-benzenecarboperoxoic acid / ethyl acetate / 5 h / 20 °C

6.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C

7.1: N,N-dimethyl-formamide / 120 h / 100 °C

8.1: potassium carbonate / N,N-dimethyl-formamide / 45 °C

With methanol; dmap; potassium tert-butylate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 3-chloro-benzenecarboperoxoic acid; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; chloroform; ethyl acetate; N,N-dimethyl-formamide; toluene;

Reference yield:

: 120-14-9
3,4-dimethoxy-benzaldehyde

: 1610859-90-9
C₃₄H₄₁Cl₂N₃O₉S

Guidance literature:: Multi-step reaction with 8 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

1.2: -78 - 20 °C

2.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 2 h / 20 °C

3.1: methanol; chloroform / 2 h / 20 °C

4.1: potassium tert-butylate; methanol / toluene / 24 h / 20 °C

5.1: 3-chloro-benzenecarboperoxoic acid / ethyl acetate / 5 h / 20 °C

6.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 °C

7.1: N,N-dimethyl-formamide / 120 h / 100 °C

8.1: potassium carbonate / N,N-dimethyl-formamide / 45 °C

With methanol; dmap; potassium tert-butylate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 3-chloro-benzenecarboperoxoic acid; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; chloroform; ethyl acetate; N,N-dimethyl-formamide; toluene;