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69304-45-6

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69304-45-6 Usage

Uses

3,5-O-(1,1,3,3-Tetraisopropyl-1,3-disiloxanediyl)adenosine (CAS# 69304-45-6) is an adenosine nucleoside used as a building block to prepare DNA and RNA duplexes with exonic splicing enhancer activity.

Check Digit Verification of cas no

The CAS Registry Mumber 69304-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,0 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69304-45:
(7*6)+(6*9)+(5*3)+(4*0)+(3*4)+(2*4)+(1*5)=136
136 % 10 = 6
So 69304-45-6 is a valid CAS Registry Number.

69304-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-[3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribofuranosyl]adenine

1.2 Other means of identification

Product number -
Other names 3',5'-O-(1,1,3,3-Tetraisopropyl- 1,3-Disloxanediyl)Adenosine

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:69304-45-6 SDS

69304-45-6Downstream Products

69304-45-6Relevant articles and documents

2′-deoxy-2′-α-C-(hydroxymethyl)adenosine as potential anti-HCV agent

Chavain, Natascha,Herdewijn, Piet

experimental part, p. 1140 - 1147 (2011/03/22)

Because of the importance of C-branched nucleosides in the discovery of new antiviral molecules, we decided to synthesize 2′-deoxy-2′-α- C-(hydroxymethyl)adenosine as a potential anti-HCV agent. The synthesis of a new adenosine analogue following two different synthetic routes is described. The new C-branched nucleoside was tested for its antiviral activity and found to be inactive.

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