Cas 369630-92-2,(17)O-labeled 6-N-benzoyl-9-(5-deoxy-3-O-diethylphosphoryl-2-O-methyl-β-D-glycero-pent-4-enofuranosyl)adenine

369630-92-2

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Basic information

Product Name: (17)O-labeled 6-N-benzoyl-9-(5-deoxy-3-O-diethylphosphoryl-2-O-methyl-β-D-glycero-pent-4-enofuranosyl)adenine
Synonyms: (17)O-labeled 6-N-benzoyl-9-(5-deoxy-3-O-diethylphosphoryl-2-O-methyl-β-D-glycero-pent-4-enofuranosyl)adenine
CAS NO:369630-92-2
Molecular Formula:
Molecular Weight: 504.452
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (17)O-labeled 6-N-benzoyl-9-(5-deoxy-3-O-diethylphosphoryl-2-O-methyl-β-D-glycero-pent-4-enofuranosyl)adenine(CAS DataBase Reference)
NIST Chemistry Reference: (17)O-labeled 6-N-benzoyl-9-(5-deoxy-3-O-diethylphosphoryl-2-O-methyl-β-D-glycero-pent-4-enofuranosyl)adenine(369630-92-2)
EPA Substance Registry System: (17)O-labeled 6-N-benzoyl-9-(5-deoxy-3-O-diethylphosphoryl-2-O-methyl-β-D-glycero-pent-4-enofuranosyl)adenine(369630-92-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 369630-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 369630-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,6,3 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 369630-92:
(8*3)+(7*6)+(6*9)+(5*6)+(4*3)+(3*0)+(2*9)+(1*2)=182
182 % 10 = 2
So 369630-92-2 is a valid CAS Registry Number.

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369630-92-2Relevant academic research and scientific papers

Dynamics of alkene radical cation/phosphate anion pair formation from nucleotide C4′ radicals. The DNA/RNA paradox revisited

Crich,Huang

, p. 9239 - 9245 (2001)

The fragmentation of nucleotide C4′ radicals generated by thiyl radical addition to C4′C5′ exocyclic glycals has been re-examined and found to be a function of the thiol and, probably, the initiating system employed. It has been demonstrated that C4′ radi

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