61074-05-3 Usage
Uses
Used in Biochemistry and Molecular Biology Research:
Cytidine periodate oxidized is used as a reagent for the selective oxidation of the 5'-hydroxyl group of ribonucleotides, facilitating various biochemical and molecular biology studies.
Used in RNA Research:
It is used as a selective labeling and modification agent for RNA molecules, which aids in the investigation of RNA structure, function, and its interactions with other biomolecules.
Used in the Preparation of Modified Nucleotides:
Cytidine periodate oxidized is utilized in the synthesis of modified nucleotides, which are essential for research applications focused on understanding and manipulating RNA properties.
Used in the Development of RNA-based Therapeutics:
CYTIDINE PERIODATE OXIDIZED is employed in the development of therapeutic agents based on RNA, potentially leading to new treatments and medicines.
Used in Nanotechnology:
Cytidine periodate oxidized has potential applications in nanotechnology, specifically for the synthesis of RNA-based nanomaterials, which could have implications in various industries such as medicine, electronics, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 61074-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,7 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61074-05:
(7*6)+(6*1)+(5*0)+(4*7)+(3*4)+(2*0)+(1*5)=93
93 % 10 = 3
So 61074-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N3O5/c10-7-1-2-12(9(16)11-7)8(5-15)17-6(3-13)4-14/h1-3,5-6,8,14H,4H2,(H2,10,11,16)/t6-,8+/m0/s1
61074-05-3Relevant academic research and scientific papers
Olsufyeva, Eugenia N.,Brusentsov, Nikolai A.,Todorova, Nedyalka,Balzarini, Jan,De Clercq, Erik,Preobrazhenskaya, Maria N.
, p. 87 - 95 (1997)
Nucleoside dialdehydes were obtained by periodate oxidation of adenosine, cytidine, guanosine, uridine or 6-azauridine in the presence of Dowex (1x8; CH3COO-). Reductive alkylation of daunorubicin with these dialdehydes in the presence of NaBH3CN produced a series of 3'-deamino-3'- (4-morpholino)daunorubicin or 13-(R,S)-dihydrodaunorubicin derivatives, the latter being mixtures of two diastereomers at 13-C atom. The morpholino- daunorubicin derivatives containing nucleic base moieties are less cytotoxic than cyanomorpholino-daunorubicin, morpholino-daunorubicin and even than the parent antibiotic.
