13992-39-7

Basic information

• Product Name: 6-(cyclohexylamino)-5-nitro-2,4(1H,3H)-pyrimidinedione
• Synonyms: 6-(cyclohexylamino)-5-nitro-2,4(1H,3H)-pyrimidinedione
• CAS NO: 13992-39-7
• Molecular Formula: C₁₀H₁₄N₄O₄
• Molecular Weight: 254.24256
• Mol File: 13992-39-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-(cyclohexylamino)-5-nitro-2,4(1H,3H)-pyrimidinedione(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(cyclohexylamino)-5-nitro-2,4(1H,3H)-pyrimidinedione(13992-39-7)
• EPA Substance Registry System: 6-(cyclohexylamino)-5-nitro-2,4(1H,3H)-pyrimidinedione(13992-39-7)

Safety Data

• Hazardous Substances Data: 13992-39-7(Hazardous Substances Data)

Upstream product

• 108-91-8 cyclohexylamine 
• 6630-30-4 6-chloro-5-nitropyrimidine-2,4(1H,3H)-dione 

Downstream Products

• 81964-47-8 8-Cyclohexyl-lumazin 

Relevant articles and documents

Pteridines, LXXI. - Synthesis and Photochemical Behaviour of 8- Substituted Lumazines

The 8-substituted lumazines 34-69 have been synthesized from 6-chloro-5-nitrouracil (1) and its 3-methyl derivative 2 via the corresponding 6-amino-5-nitrouracils 3-26, substituted at the amino nitrogen.The photochemical properties of the 8-substituted lumazines have been investigated.Various photoreactions were observed depending on the chemical nature of the N-8-side-chain and leading to an easy photodealkylation of the β-hydroxy-, β-methoxy-, and β-aminoethyl derivatives 34-44.Increasing donor properties of the β-substituent enhances the photolability which is expressed in a Norrish-type II cleavage reaction to the corresponding lumazines 70-75. 8-Cycloalkyllumazines 52-54 show photoreduction to 7,8-dihydrolumazines 76-78.The newly synthesized 8-substituted lumazine derivatives have been characterized by elementary analyses and UV spectra.Structural peculiarities due to the various substituents in position 6, 7, and 8 will be discussed.