Production Method 1

298-46-4

1095650-06-8

6915-15-7

36507-30-9

1177432-69-7

885-23-4

578-95-0

77-92-9

106680-74-4

1391124-13-2

526-83-0

537693-29-1

Reaction Conditions

1.1R:Oxone, C:125825-47-0, C:25014-41-9, C:Poly-4-vinylpyridine, S:H2O, rt, pH 7

Reference

High-Valent Iron-Oxo Complexes as Dominant Species to Eliminate Pharmaceuticals and Chloride-Containing Intermediates by the Activation of Peroxymonosulfate Under Visible Irradiation

By Zhu, Zhexin et al, Catalysis Letters, 2020, 150(5), 1355-1367

4-Formyl-9-oxo-10(9H)-acridinecarboxamide Raw materials

• Carbamazepine

4-Formyl-9-oxo-10(9H)-acridinecarboxamide Preparation Products

• Malic acid (6915-15-7)
• 1a,10b-dihydro-6H-dibenzo[b,f]oxireno[2,3-d]azepine-6-carboxamide (36507-30-9)
• 9-Oxo-10(9H)-acridinecarboxaldehyde (1177432-69-7)
• acridine-9-carbaldehyde (885-23-4)
• Acridone (578-95-0)
• Citric acid (77-92-9)
• (106680-74-4)
• Urea, N,N-bis(2-formylphenyl)- (1391124-13-2)
• DL-Tartaric acid (526-83-0)
• 11-Keto Oxcarbazepine (537693-29-1)
• 4-Formyl-9-oxo-10(9H)-acridinecarboxamide (1095650-06-8)

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  Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
• 5. Alternative donor substrates for inverting and retaining glycosyltransferases?
  Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367

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