70523-27-2 Usage
General Description
2,4-bis(benzyloxy)-6-bromopyrimidine is a chemical compound with the molecular formula C18H16BrN2O2. It is a pyrimidine derivative that contains two benzyloxy groups and a bromine atom. 2,4-bis(benzyloxy)-6-bromopyrimidine has potential applications in medicinal chemistry, particularly in the development of pharmaceutical drugs. It may also be used as a building block in the synthesis of various organic molecules. Additionally, 2,4-bis(benzyloxy)-6-bromopyrimidine is a valuable tool for researchers and scientists in the field of organic chemistry due to its diverse reactivity and potential for structural modification. Overall, 2,4-bis(benzyloxy)-6-bromopyrimidine has significant relevance in both the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 70523-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,2 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70523-27:
(7*7)+(6*0)+(5*5)+(4*2)+(3*3)+(2*2)+(1*7)=102
102 % 10 = 2
So 70523-27-2 is a valid CAS Registry Number.
70523-27-2Relevant academic research and scientific papers
Syntheses of the cylindrospermopsin alkaloids
Looper, Ryan E.,Runnegar, Maria T.C.,Williams, Robert M.
, p. 4549 - 4562 (2007/10/03)
An intramolecular 1,3-dipolar cycloaddition has efficiently constructed the A-ring portions of the cylindrospermopsin alkaloids. A nitro-aldol addition of an elaborated nitroalkane to a pyrimidine aldehyde followed by an intramolecular reductive guanidiny
Synthesis of the putative structure of 7-deoxycylindrospermopsin: C7 oxygenation is not required for the inhibition of protein synthesis
Looper, Ryan E.,Runnegar, Maria T. C.,Williams, Robert M.
, p. 3879 - 3881 (2007/10/03)
(Chemical Equation Presented) Naturally occurring! The cyanobacterial metabolite 7-deoxycylindrospermopsin has been synthesized and its natural occurrence confirmed by HPLC. Structural analysis and protein-inhibition studies show that the uracil unit does