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7-(2,3,5-tri-O-acetylpentofuranosyl)-1,7-dihydro-4H-imidazo[4,5-d][1,2,3]triazin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36519-17-2

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36519-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36519-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,1 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36519-17:
(7*3)+(6*6)+(5*5)+(4*1)+(3*9)+(2*1)+(1*7)=122
122 % 10 = 2
So 36519-17-2 is a valid CAS Registry Number.

36519-17-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,4-diacetyloxy-5-(4-oxo-1H-imidazo[4,5-d]triazin-7-yl)oxolan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names 7-(2,3,5-tri-o-acetylpentofuranosyl)-1,7-dihydro-4h-imidazo[4,5-d][1,2,3]triazin-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36519-17-2 SDS

36519-17-2Downstream Products

36519-17-2Relevant academic research and scientific papers

Purine nucleoside analogues for treating flaviviridae including hepatitis C

-

Page/Page column 82, (2016/02/05)

This invention is directed to a method for treating a host, especially a human, infected with hepatitis C, flavivirus and/or pestivirus, comprising administering to that host an effective amount of an anti-HCV biologically active pentofuranonucleoside whe

Practical synthesis of natural plant-growth regulator 2-azahypoxanthine, its derivatives, and biotin-labeled probes

Ikeuchi, Kazutada,Fujii, Ryosuke,Sugiyama, Shimpei,Asakawa, Tomohiro,Inai, Makoto,Hamashima, Yoshitaka,Choi, Jae-Hoon,Suzuki, Tomohiro,Kawagishi, Hirokazu,Kan, Toshiyuki

supporting information, p. 3813 - 3815 (2014/06/09)

We describe a practical, large-scale synthesis of the "fairy- ring" plant-growth regulator 2-azahypoxanthine (AHX), and its biologically active hydroxyl metabolite (AOH) and riboside derivative (AHXr). AHXr, a biosynthetic intermediate, was synthesized from inosine via a biomimetic route. Biotinylated derivatives of AHX and AHXr were also synthesized as probes for mechanistic studies. This journal is the Partner Organisations 2014.

Synthesis and biophysical and biological properties of oligonucleotides containing 2-aza-2'-deoxyinosine

Acedo,De Clercq,Eritja

, p. 6262 - 6269 (2007/10/03)

The preparation of oligonucleotides containing 2-aza-2'-deoxyinosine is described. Protection of the 2-azahypoxanthine moiety with the photolabile 2-nitrobenzyl group enabled us to obtain the phosphoramidite derivative and oligonucleotides containing protected 2-aza-2'-deoxyinosine. After purification, photolysis of the oligonucleotides containing the protected analogue provided the desired oligonucleotides in good yields. Melting curves of duplexes containing 2-azahypoxanthine paired with the four natural bases at pH 6 and pH 8 proved that 2-azahypoxanthine base pairs were less stable than perfectly matched duplexes but showed little variation among different bases.

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