128499-41-2

Basic information

• Product Name: 2,4(1H,3H)-Pyrimidinedione, 5-[(2-aminophenyl)thio]-1,3-dimethyl-
• CAS NO: 128499-41-2
• Molecular Formula: C12H13N3O2S
• Molecular Weight: 263.32
• Mol File: 128499-41-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,4(1H,3H)-Pyrimidinedione, 5-[(2-aminophenyl)thio]-1,3-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 5-[(2-aminophenyl)thio]-1,3-dimethyl-(128499-41-2)
• EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 5-[(2-aminophenyl)thio]-1,3-dimethyl-(128499-41-2)

Safety Data

• Hazardous Substances Data: 128499-41-2(Hazardous Substances Data)

Upstream product

• 49846-86-8 6-cyano-1,3-dimethyluracil 
• 137-07-5 2-amino-benzenethiol 
• 7033-39-8 5-bromo-1,3-dimethyluracil 

Relevant articles and documents

Umpolung of Reactivity at the C-5 Position of Uracil: Facile Nucleophilic Reactions of Thiolate Ions at C-5 of 6-Cyano-1,3-dimethyluracil to Procure 5-Alkyl or 5-aryl-thio-1,3-dimethyluracils

1,3-Dimethyluracil-6-carbonitrile 1 with thiolate ions generated in situ from thioiminium salts or thiols under phase transfer catalytic conditions undergoes umpolung of reactivity at C-5 to give 5-alkyl- or 5-aryl-thio-1,3-dimethyluracils as the major or sole products.However, propane-1,3-dithiol causes reductive decyanation of 1 to 1,3-dimethyluracil.

Reactions of diazenes with nucleophiles: Part II- Facile one step conversion of 5-bromo-1,3-dimethyluracil to 5-alkyl/aryl-thio-and 6-alkylthio-1,3-dimethyluracil derivatives

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