24616-99-7 Usage
Chemical structure
A complex chemical compound with a unique structure consisting of a pyridinone ring attached to a pentofuranosyl group.
Substituents
Contains two 4-methylbenzoyl groups attached to the pentofuranosyl group at the 3-O and 5-O positions.
Stereochemistry
The compound has an α-D-erythro configuration.
Potential applications
Has potential applications in the pharmaceutical industry due to its complex structure and potential biological activity.
Drug development
May have the potential for use in drug development due to its unique structure and possible pharmacological properties.
Further research
More research is needed to fully understand the potential uses and effects of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 24616-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,1 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24616-99:
(7*2)+(6*4)+(5*6)+(4*1)+(3*6)+(2*9)+(1*9)=117
117 % 10 = 7
So 24616-99-7 is a valid CAS Registry Number.
24616-99-7Relevant academic research and scientific papers
Glycosylations of Ambident Anions of 2(1H)- and 4(1H)-Pyridone and Stereoselective Synthesis of 2(1H)-Pyrimidinone N-(2'-Deoxy-α-D-ribofuranoside)
Seela, Frank,Bindig, Uwe
, p. 895 - 902 (2007/10/02)
Glycosylation of the ambident anions of 2(1H)-pyridone (6) and 4(1H)-pyridone (11) in the presence of KOH with 2-deoxy-3,5-di-O-(p-toluoyl)-α-D-erythro-pentofuranosyl chloride (7) stereoselectively yielded the β-D-O-glycosides 8 and 12, together with anom
