Production Method 1

83921-18-0

141-82-2

617-45-8

6915-15-7

80-69-3

2577-38-0

134434-28-9

1068-84-4

66-22-8

496-76-4

57-13-6

68-94-0

65-86-1

73-24-5

73-40-5

79-14-1

110-15-6

932-52-5

56-40-6

Reaction Conditions

1.1 Reagents: Ammonium chloride Solvents: Water ;  3 - 30 d, 38 °C
1.2 Reagents: Hydrochloric acid Solvents: Water ;  24 h, 110 °C

Reference

New Insights into the Characterization of 'Insoluble Black HCN Polymers'

Ruiz-Bermejo, Marta; de la Fuente, Jose L.; Rogero, Celia; Menor-Salvan, Cesar; Osuna-Esteban, Susana; et al, Chemistry & Biodiversity, 2012, 9(1), 25-40

Pyrimidine, 2,3,4,5-tetrahydro- Preparation Products

• propanedioic acid (141-82-2)
• 2-aminobutanedioic acid (617-45-8)
• Malic acid (6915-15-7)
• Hydroxymalonic Acid (80-69-3)
• 2,4,7(1H,3H,8H)-Pteridinetrione (2577-38-0)
• Pyrazine-2,5-diol (134434-28-9)
• 2-Aminomalonic Acid Monopotassium Salt (1068-84-4)
• Uracil (66-22-8)
• Isobarbituric Acid (496-76-4)
• Urea (57-13-6)
• Hypoxanthine (68-94-0)
• 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid (65-86-1)
• Adenine (73-24-5)
• Guanine (73-40-5)
• 2-hydroxyacetic acid (79-14-1)
• butanedioic acid (110-15-6)
• 5-Aminouracil (932-52-5)
• Glycine (56-40-6)
• Pyrimidine, 2,3,4,5-tetrahydro- (83921-18-0)

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