C₆₆H₁₀₄N₄O₁₂S₂

Base Information

Chemical Name:C₆₆H₁₀₄N₄O₁₂S₂
CAS No.:1280727-40-3
Molecular Formula:C₆₆H₁₀₄N₄O₁₂S₂
Molecular Weight:1209.7
Hs Code.:

C<sub>66</sub>H<sub>104</sub>N<sub>4</sub>O<sub>12</sub>S<sub>2</sub>

Synonyms:C₆₆H₁₀₄N₄O₁₂S₂

Suppliers and Price of C₆₆H₁₀₄N₄O₁₂S₂

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of C₆₆H₁₀₄N₄O₁₂S₂

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₆₆H₁₀₄N₄O₁₂S₂

There total 9 articles about C₆₆H₁₀₄N₄O₁₂S₂ 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:

: 1280727-36-7
C₃₃H₅₄N₂O₅S

: 1280727-39-0
C₃₃H₅₂N₂O₈S

: 1280727-40-3
C₆₆H₁₀₄N₄O₁₂S₂

Guidance literature:: C₃₃H₅₄N₂O₅S; C₃₃H₅₂N₂O₈S; In acetic anhydride; at 20 ℃;

With trifluoroacetic acid; In acetic anhydride; at 20 ℃; for 3h; Cooling with ice;

With pyridine; sodium hydrogencarbonate; In water; acetic anhydride; at 20 ℃; for 3h; Product distribution / selectivity;

Reference yield:

: 563-80-4
3-methyl-butan-2-one

: 1280727-40-3
C₆₆H₁₀₄N₄O₁₂S₂

Guidance literature:: Multi-step reaction with 7 steps

1.1: bromine; hydrogen bromide / water; methanol / 3.5 h / 30 - 34 °C

2.1: water; ISOPROPYLAMIDE / 4 h / 20 °C

3.1: methanol / Inert atmosphere

3.2: 8 h / 20 °C / Reflux

4.1: ISOPROPYLAMIDE / 3 h / 20 °C

5.1: 1-methyl-pyrrolidin-2-one / 20 °C

5.2: 2 h / 20 °C

6.1: nitrobenzene / ISOPROPYLAMIDE / 2 h / 20 °C

7.1: acetic anhydride / 20 °C

7.2: 3 h / 20 °C / Cooling with ice

7.3: 3 h / 20 °C

With hydrogen bromide; bromine; nitrobenzene; In 1-methyl-pyrrolidin-2-one; methanol; ISOPROPYLAMIDE; water; acetic anhydride;

Reference yield:

: 17687-64-8
2-(3-methyl-2-oxobutyl)isoindoline-1,3-dione

: 1280727-40-3
C₆₆H₁₀₄N₄O₁₂S₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: methanol / Inert atmosphere

1.2: 8 h / 20 °C / Reflux

2.1: ISOPROPYLAMIDE / 3 h / 20 °C

3.1: 1-methyl-pyrrolidin-2-one / 20 °C

3.2: 2 h / 20 °C

4.1: nitrobenzene / ISOPROPYLAMIDE / 2 h / 20 °C

5.1: acetic anhydride / 20 °C

5.2: 3 h / 20 °C / Cooling with ice

5.3: 3 h / 20 °C

With nitrobenzene; In 1-methyl-pyrrolidin-2-one; methanol; ISOPROPYLAMIDE; acetic anhydride;