Cas 107796-03-2,1,5-anhydro-2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-D-ribo-hex-1-enitol

107796-03-2

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Basic information

Product Name: 1,5-anhydro-2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-D-ribo-hex-1-enitol
Synonyms: 1,5-anhydro-2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-D-ribo-hex-1-enitol
CAS NO:107796-03-2
Molecular Formula:
Molecular Weight: 593.46
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: 1,5-anhydro-2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-D-ribo-hex-1-enitol(CAS DataBase Reference)
NIST Chemistry Reference: 1,5-anhydro-2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-D-ribo-hex-1-enitol(107796-03-2)
EPA Substance Registry System: 1,5-anhydro-2-deoxy-3,4,6-tris-O-(4-nitrobenzoyl)-D-ribo-hex-1-enitol(107796-03-2)

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: 107796-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107796-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107796-03:
(8*1)+(7*0)+(6*7)+(5*7)+(4*9)+(3*6)+(2*0)+(1*3)=142
142 % 10 = 2
So 107796-03-2 is a valid CAS Registry Number.

107796-03-2Upstream product

107796-03-2Downstream Products

107796-03-2Relevant 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 (2007/10/02)

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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