85879-00-1 Usage
Structure
Complex structure with a hexitol ring, a chlorine atom, and a 6-methoxy-2-methylpyrimidin-4-yl group The compound has a complex structure that includes a hexitol ring, which is a sugar molecule with six carbon atoms, a chlorine atom, and a 6-methoxy-2-methylpyrimidin-4-yl group, which is an organic molecule that contains a pyrimidine ring with a methoxy and a methyl group attached.
Use in pharmaceutical research and drug development
Valuable tool for studying biological processes and potential drug interactions The unique structure and properties of 2,5-anhydro-1-chloro-1-deoxy-1-(6-methoxy-2-methylpyrimidin-4-yl)hexitol make it a valuable tool for studying biological processes and potential drug interactions.
Potential therapeutic applications
Interaction with biological systems 2,5-anhydro-1-chloro-1-deoxy-1-(6-methoxy-2-methylpyrimidin-4-yl)hexitol may have potential therapeutic applications due to its interaction with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 85879-00-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,7 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85879-00:
(7*8)+(6*5)+(5*8)+(4*7)+(3*9)+(2*0)+(1*0)=181
181 % 10 = 1
So 85879-00-1 is a valid CAS Registry Number.
85879-00-1Relevant academic research and scientific papers
Synthesis of Homo-C-nucleosides using Pyrimidinylmethylenephosphoranes
Katagiri, Nobuya,Takashima, Kenichi,Kato, Tetsuzo,Sato, Sadao,Tamura, Chihiro
, p. 201 - 209 (2007/10/02)
The direct synthesis of homo-C-nucleosides from pyrimidinylmethylenephosphoranes and protected D-ribose is described.Reaction of 2,3-O-isopropylidene-5-O-trityl-D-ribose (9) with pyrimidinylmethylenephosphoranes (5)-(8) gave protected α-and β-homo-C-nucleosides (14)-(21) and pyrimidinylolefins (10)-(13) in good yields.The ratio of α- and β-nucleosides depended on the properties of phosphoranes.Treatment of compounds (10)-(13) with base such as triethylamine or 1,8-diazabicycloundec-7-ene (DBU) gave ring-closed products (14)-(21) in quantitative yields.Deprotection of compounds (14)-(21) with hydrochloric acid in either dioxane-water or methanol gave homo-C-nucleosides (22)-(32).
