Cas 144427-87-2,3-<2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl>-4-(methylthio)-1H-imidazo<4,5-c>pyridine

144427-87-2

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Basic information

Product Name: 3-<2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl>-4-(methylthio)-1H-imidazo<4,5-c>pyridine
Synonyms: 3-<2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl>-4-(methylthio)-1H-imidazo<4,5-c>pyridine
CAS NO:144427-87-2
Molecular Formula:
Molecular Weight: 517.605
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: 3-<2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl>-4-(methylthio)-1H-imidazo<4,5-c>pyridine(CAS DataBase Reference)
NIST Chemistry Reference: 3-<2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl>-4-(methylthio)-1H-imidazo<4,5-c>pyridine(144427-87-2)
EPA Substance Registry System: 3-<2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl>-4-(methylthio)-1H-imidazo<4,5-c>pyridine(144427-87-2)

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: 144427-87-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144427-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,2 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144427-87:
(8*1)+(7*4)+(6*4)+(5*4)+(4*2)+(3*7)+(2*8)+(1*7)=132
132 % 10 = 2
So 144427-87-2 is a valid CAS Registry Number.

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144427-87-2Relevant academic research and scientific papers

3-Deaza-2'-deoxyadenosine: Synthesis via 4-(Methylthio)-1H-imidazopyridine 2'-Deoxyribonucleosides and Properties of Oligonucleotides

Seela, Frank,Grein, Thomas,Samnick, Samuel

, p. 1639 - 1650 (1992)

The synthesis of 4-(methylthio)-1H-imidazopyridine 2'-deoxy-β-D-ribonucleosides 2 and 9 and the conversion of the N1-isomer 2 into the 2',3'-didehydro-2',3'-dideoxyribonucleoside 3a or (via 7) 3-deaza-2'-deoxyadenosine (1) is described.P

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