C₆₀H₈₈N₆O₁₀S

Base Information

Chemical Name:C₆₀H₈₈N₆O₁₀S
CAS No.:271800-38-5
Molecular Formula:C₆₀H₈₈N₆O₁₀S
Molecular Weight:1085.46
Hs Code.:

C<sub>60</sub>H<sub>88</sub>N<sub>6</sub>O<sub>10</sub>S

Synonyms:C₆₀H₈₈N₆O₁₀S

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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 C₆₀H₈₈N₆O₁₀S

Chemical Property:

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Technology Process of C₆₀H₈₈N₆O₁₀S

There total 6 articles about C₆₀H₈₈N₆O₁₀S 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:

: 39021-83-5
3,6-dimethoxy-o-xylene

: 271800-38-5
C₆₀H₈₈N₆O₁₀S

Guidance literature:: Multi-step reaction with 6 steps

1.1: 61 percent / Nh₄NO₃; trifluoroacetic anhydride / acetonitrile / 2.5 h / 20 °C

2.1: 96 percent / H₂ / Ra-Ni / tetrahydrofuran / 18 h

3.1: SO₂NH₂ / bis-(2-methoxy-ethyl) ether / Heating

3.2: 41 percent / DMAP / 24 h / 20 °C

4.1: 100 percent / N-bromosuccinimide / CCl₄ / 1.5 h / Heating

5.1: KO-t-Bu

6.1: cerium ammonium nitrate

With ammonium nitrate; N-Bromosuccinimide; ammonium cerium(IV) nitrate; potassium tert-butylate; hydrogen; SULFAMIDE; trifluoroacetic anhydride; Ra-Ni; In tetrahydrofuran; tetrachloromethane; diethylene glycol dimethyl ether; acetonitrile; 1.1: Substitution / 2.1: Catalytic hydrogenation / 3.1: Cyclization / 3.2: Acylation / 4.1: Bromination / 5.1: Substitution / 5.2: Cyclization / 6.1: Oxidation;
DOI:10.1021/ja0005136

Reference yield:

: 186039-76-9
1,4-dimethoxy-5,6-dimethyl-2,3-dinitrobenzene

: 271800-38-5
C₆₀H₈₈N₆O₁₀S

Guidance literature:: Multi-step reaction with 5 steps

1.1: 96 percent / H₂ / Ra-Ni / tetrahydrofuran / 18 h

2.1: SO₂NH₂ / bis-(2-methoxy-ethyl) ether / Heating

2.2: 41 percent / DMAP / 24 h / 20 °C

3.1: 100 percent / N-bromosuccinimide / CCl₄ / 1.5 h / Heating

4.1: KO-t-Bu

5.1: cerium ammonium nitrate

With N-Bromosuccinimide; ammonium cerium(IV) nitrate; potassium tert-butylate; hydrogen; SULFAMIDE; Ra-Ni; In tetrahydrofuran; tetrachloromethane; diethylene glycol dimethyl ether; 1.1: Catalytic hydrogenation / 2.1: Cyclization / 2.2: Acylation / 3.1: Bromination / 4.1: Substitution / 4.2: Cyclization / 5.1: Oxidation;
DOI:10.1021/ja0005136

Reference yield:

: 186039-77-0
1,4-dimethoxy-5,6-dimethyl-2,3-diaminobenzene

: 271800-38-5
C₆₀H₈₈N₆O₁₀S

Guidance literature:: Multi-step reaction with 4 steps

1.1: SO₂NH₂ / bis-(2-methoxy-ethyl) ether / Heating

1.2: 41 percent / DMAP / 24 h / 20 °C

2.1: 100 percent / N-bromosuccinimide / CCl₄ / 1.5 h / Heating

3.1: KO-t-Bu

4.1: cerium ammonium nitrate

With N-Bromosuccinimide; ammonium cerium(IV) nitrate; potassium tert-butylate; SULFAMIDE; In tetrachloromethane; diethylene glycol dimethyl ether; 1.1: Cyclization / 1.2: Acylation / 2.1: Bromination / 3.1: Substitution / 3.2: Cyclization / 4.1: Oxidation;
DOI:10.1021/ja0005136