86958-61-4

Basic information

• Product Name: 2H-Pyran, 2,2'-[(2,3-dimethyl-2,3-dinitro-1,4-butanediyl)bis(oxy)]bis[tetrahydro-
• CAS NO: 86958-61-4
• Molecular Formula: C16H28N2O8
• Molecular Weight: 376.407
• Mol File: 86958-61-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2H-Pyran, 2,2'-[(2,3-dimethyl-2,3-dinitro-1,4-butanediyl)bis(oxy)]bis[tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran, 2,2'-[(2,3-dimethyl-2,3-dinitro-1,4-butanediyl)bis(oxy)]bis[tetrahydro-(86958-61-4)
• EPA Substance Registry System: 2H-Pyran, 2,2'-[(2,3-dimethyl-2,3-dinitro-1,4-butanediyl)bis(oxy)]bis[tetrahydro-(86958-61-4)

Safety Data

• Hazardous Substances Data: 86958-61-4(Hazardous Substances Data)

Upstream product

• 109178-34-9 2-(2-Bromo-2-nitro-propoxy)-tetrahydro-pyran 
• 71-30-7 Cytosine 

Relevant articles and documents

Selective N1-alkylation of pyrimidine bases via radical (S(RN)1) mechanism

Under photostimulated S(RN)1 conditions the cytosine nitranion behaves as a nucleophile toward the carbon radical generated from gem halonitro, or gem dinitroalcane derivatives to give regiospecifically the N-1 alkyled cytosine compound which is representative of a new series of cytosine acyclonucleosides. Uracile and its 5-fluoro or 5-nitro analogs fail to react and thymine gives an unexpected disubstituted S(RN)1 product whose formation is discussed.