Cas 6129-68-6,1-(2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-β-D-ribo-hexopyranosyl)-2,4-pyrimidinedione

6129-68-6

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Basic information

Product Name: 1-(2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-β-D-ribo-hexopyranosyl)-2,4-pyrimidinedione
Synonyms: 1-(2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-β-D-ribo-hexopyranosyl)-2,4-pyrimidinedione
CAS NO:6129-68-6
Molecular Formula:
Molecular Weight: 705.548
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: 1-(2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-β-D-ribo-hexopyranosyl)-2,4-pyrimidinedione(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-β-D-ribo-hexopyranosyl)-2,4-pyrimidinedione(6129-68-6)
EPA Substance Registry System: 1-(2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-β-D-ribo-hexopyranosyl)-2,4-pyrimidinedione(6129-68-6)

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: 6129-68-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6129-68-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6129-68:
(6*6)+(5*1)+(4*2)+(3*9)+(2*6)+(1*8)=96
96 % 10 = 6
So 6129-68-6 is a valid CAS Registry Number.

6129-68-6Upstream product

6129-68-6Downstream Products

6067-31-8 1-(2-deoxy-β-D-ribo-hexopyranosyl)-2,4-pyrimidinedione

6129-68-6Relevant academic research and scientific papers

Synthesis, Structure, and Biological Activity of Certain 2-Deoxy-β-D-ribo-hexopyranosyl Nucleosides and Nucleotides

Nord, L. Dee,Dalley, N. Kent,McKernan, Patricia A.,Robins, Roland K.

, p. 1044 - 1054 (1987)

2-Deoxy-β-D-ribo-hexopyranosyl nucleosides with adenine (2), hypoxanthine (17), guanine (23), cytosine (13), and uracil (7) as the aglycon were synthesized by the Lewis-acid-catalyzed condensation of an appropriate trimethylsilylated heterocyclic base and

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