Cas 181259-75-6,Benzoic acid (2R,3R,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-{hydroxy-[2-(4-nitro-phenyl)-ethoxy]-phosphoryloxy}-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester

181259-75-6

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Basic information

Product Name: Benzoic acid (2R,3R,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-{hydroxy-[2-(4-nitro-phenyl)-ethoxy]-phosphoryloxy}-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester
Synonyms:
CAS NO:181259-75-6
Molecular Formula:
Molecular Weight: 962.953
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: Benzoic acid (2R,3R,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-{hydroxy-[2-(4-nitro-phenyl)-ethoxy]-phosphoryloxy}-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2R,3R,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-{hydroxy-[2-(4-nitro-phenyl)-ethoxy]-phosphoryloxy}-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester(181259-75-6)
EPA Substance Registry System: Benzoic acid (2R,3R,4R,5R)-5-(6-benzylamino-purin-9-yl)-4-{hydroxy-[2-(4-nitro-phenyl)-ethoxy]-phosphoryloxy}-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester(181259-75-6)

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: 181259-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 181259-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,2,5 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 181259-75:
(8*1)+(7*8)+(6*1)+(5*2)+(4*5)+(3*9)+(2*7)+(1*5)=146
146 % 10 = 6
So 181259-75-6 is a valid CAS Registry Number.

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181259-75-6Relevant academic research and scientific papers

N6-benzyladenosine analogs of (A2′p)2A: Synthesis and activity to tobacco mosaic virus

Kvasyuk,Kulak,Zinchenko,Barai,Mikhailopulo

, p. 181 - 187 (2007/10/03)

Analogs of (2′-5′)oligoadenylate trimer with N6-benzyladenosine in various positions of the chain and the fully substituted trimer were synthesized by the phosphotriester method. The structures of compounds prepared were proved by UV, CD, and 1H NMR. The obtained substances inhibit replication of tobacco mosaic virus at a 10-8-10-6 M concentration, which is comparable with that of natural (A2′p)2A triadenylate.

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