Cas 916346-29-7,6-[6-phenyl-2-cyano-2-(carboethoxy)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine

916346-29-7

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Basic information

Product Name: 6-[6-phenyl-2-cyano-2-(carboethoxy)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine
Synonyms: 6-[6-phenyl-2-cyano-2-(carboethoxy)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine
CAS NO:916346-29-7
Molecular Formula:
Molecular Weight: 667.675
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-[6-phenyl-2-cyano-2-(carboethoxy)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine(CAS DataBase Reference)
NIST Chemistry Reference: 6-[6-phenyl-2-cyano-2-(carboethoxy)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine(916346-29-7)
EPA Substance Registry System: 6-[6-phenyl-2-cyano-2-(carboethoxy)indan-5-yl]-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine(916346-29-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 916346-29-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 916346-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,3,4 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 916346-29:
(8*9)+(7*1)+(6*6)+(5*3)+(4*4)+(3*6)+(2*2)+(1*9)=177
177 % 10 = 7
So 916346-29-7 is a valid CAS Registry Number.

916346-29-7Upstream product

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916346-29-7Relevant academic research and scientific papers

Preparation of highly substituted 6-arylpurine ribonucleosides by Ni-catalyzed cyclotrimerization. Scope of the reaction

Turek, Pavel,Novak, Petr,Pohl, Radek,Hocek, Michal,Kotora, Martin

, p. 8978 - 8981 (2007/10/03)

Transition metal complex catalyzed cocyclotrimerization of protected alkynylpurine ribonucleosides 1 with various diynes 2 gave rise to a series of 6-arylpurine nucleosides 3 that were further deprotected to free nucleosides 4. Generally, the best yields

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