Cas 1312701-75-9,6-amino-1-(2-deoxy-β-D-erythropentofuranosyl)-1,5-dihydro-3-[1-(4-azidomethylbenzyl)-1H-[1,2,3-triazol-4-yl]]-4H-pyrazolo[3,4-d]pyrimidin-4-one

1312701-75-9

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Product Name: 6-amino-1-(2-deoxy-β-D-erythropentofuranosyl)-1,5-dihydro-3-[1-(4-azidomethylbenzyl)-1H-[1,2,3-triazol-4-yl]]-4H-pyrazolo[3,4-d]pyrimidin-4-one
Synonyms: 6-amino-1-(2-deoxy-β-D-erythropentofuranosyl)-1,5-dihydro-3-[1-(4-azidomethylbenzyl)-1H-[1,2,3-triazol-4-yl]]-4H-pyrazolo[3,4-d]pyrimidin-4-one
CAS NO:1312701-75-9
Molecular Formula:
Molecular Weight: 479.458
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: 6-amino-1-(2-deoxy-β-D-erythropentofuranosyl)-1,5-dihydro-3-[1-(4-azidomethylbenzyl)-1H-[1,2,3-triazol-4-yl]]-4H-pyrazolo[3,4-d]pyrimidin-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 6-amino-1-(2-deoxy-β-D-erythropentofuranosyl)-1,5-dihydro-3-[1-(4-azidomethylbenzyl)-1H-[1,2,3-triazol-4-yl]]-4H-pyrazolo[3,4-d]pyrimidin-4-one(1312701-75-9)
EPA Substance Registry System: 6-amino-1-(2-deoxy-β-D-erythropentofuranosyl)-1,5-dihydro-3-[1-(4-azidomethylbenzyl)-1H-[1,2,3-triazol-4-yl]]-4H-pyrazolo[3,4-d]pyrimidin-4-one(1312701-75-9)

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Hazardous Substances Data: 1312701-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312701-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1312701-75:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*0)+(3*1)+(2*7)+(1*5)=109
109 % 10 = 9
So 1312701-75-9 is a valid CAS Registry Number.

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1312701-75-9Relevant academic research and scientific papers

Stepwise "click" chemistry for the template independent construction of a broad variety of cross-linked oligonucleotides: Influence of linker length, position, and linking number on DNA duplex stability

Xiong, Hai,Seela, Frank

, p. 5584 - 5597 (2011/09/12)

Cross-linked DNA was constructed by a "stepwise click" reaction using a bis-azide. The reaction is performed in the absence of a template, and a monofunctionalized oligonucleotide bearing an azido-function is formed as intermediate. For this, an excess of

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