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4-(6-AMINO-9H-PURIN-9-YL)-2,5-ANHYDRO-6-AZIDO-4,6-DIDEOXY-DIMETHYL ACETAL-L-MANNOSE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

944475-14-3

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944475-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 944475-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,4,7 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 944475-14:
(8*9)+(7*4)+(6*4)+(5*4)+(4*7)+(3*5)+(2*1)+(1*4)=193
193 % 10 = 3
So 944475-14-3 is a valid CAS Registry Number.

944475-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R,4R,5S)-4-(6-amino-9H-purin-9-yl)-5-(azidomethyl)-2-(dimethoxymethyl)tetrahydrofuran-3-ol

1.2 Other means of identification

Product number -
Other names -

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:944475-14-3 SDS

944475-14-3Downstream Products

944475-14-3Relevant academic research and scientific papers

Studies on modified oligonucleotides

Zhang, Li He,Yang, Zhen Jun,Zhang, Liang Ren

body text, p. 326 - 334 (2009/05/07)

A series of isonucleotide incorporated antisense oligodeoxynucleotides have been synthesized, in which isonucleotide was introduced at different positions of the sequences. The results showed that though the incorporated isonucleotides at different position of the sequence interfered in the binding ability in different extent, B-form duplexes were maintained and the binding abilities of the 3′-end modified duplexes were better than the corresponding mismatched duplexes. The DNA/RNA hybrid formed by modified oligodeoxynucleotide and its target RNA could activate the activity of RNase H. The 3′-end modified antisense oligodeoxynucelotides showed the inhibition on S glycoprotein expression of SARS-CoV at the mRNA levels in insect Sf9 cells. In this presentation, a novel class of amino-isonucleoside was synthesized and incorporated into different positions in the sense or antisense strand of siRNA duplexes. The 3′ and 5′ sense strand aminonucleoside modified siRNAs (ssISO-siRNA1 and ssISO-siRNA2) showed the similar duplex thermal and serum stability as natural one and the luciferase activities showed that such modified siRNA is compatible with the intracellular siRNA machinery. Copyright Taylor & Francis Group, LLC.

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