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3593-47-3

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  • 5'- Phosphoadenylyl- (3' → 5')- adenosine ( pApA )

    Cas No: 3593-47-3

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3593-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3593-47-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3593-47:
(6*3)+(5*5)+(4*9)+(3*3)+(2*4)+(1*7)=103
103 % 10 = 3
So 3593-47-3 is a valid CAS Registry Number.

3593-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name D,D-pA(3'-5')pA

1.2 Other means of identification

Product number -
Other names 5'-phosphoadenylyl-(3'->5')-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:3593-47-3 SDS

3593-47-3Downstream Products

3593-47-3Relevant articles and documents

Mechanism of montmorillonite catalysis in the formation of RNA oligomers

Joshi, Prakash C.,Aldersley, Michael F.,Delano, John W.,Ferris, James P.

, p. 13369 - 13374 (2009)

The montmorillonite clay-catalyzed reactions of nucleotides generate oligomers as long as 50-mers. The extent of catalysis depends on the magnitude of the negative charge on the montmorillonite lattice and the number of cations associated with it. When ca

Kinetic and mechanistic analysis of dinucleotide and oligonucleotide formation from the 5′-phosphorimidazolide of adenosine on Na+-montmorillonite

Kawamura, Kunio,Ferris, James P.

, p. 7564 - 7572 (2007/10/02)

The rate constants for the condensation reaction of the 5′-phosphorimidazolide of adenosine (ImpA) to form dinucleotides and oligonucleotides have been measured in the presence of Na+-volclay (a Na+-montmorillonite) in pH 8 aqueous solution at 25 °C. The rates of the reaction of ImpA with an excess of adenosine 5′-monophosphoramidate (NH2pA), .P1,P2-diadenosine 5′,5′-pyrophosphate (A5′ppA), or adenosine 5′-monophosphate (5′-AMP or pA) in the presence of the montmorillonite to form NH2pA3′pA, A5′ppA3′pA, and pA3′pA, respectively, were measured. Only 3′,5′-linked products were observed. The magnitude of the rate constants decrease in the order NH2pA3′pA > A5′-ppA3′pA > pA3′pA. The binding of ImpA to montmorillonite was measured, and the adsorption isotherm was determined. The binding of ImpA to montmorillonite and the formation of higher oligonucleotides is not observed in the absence of salts. Mg2+ enhances binding and oligonucleotide formation more than Ca2+ and Na+. The rate constants for the oligonucleotide formation were determined from the reaction products formed from 10 to 40 mM ImpA in the presence of Na+-montmorillonite using the computer program SIMFIT. The magnitudes of the rate constants for the formation of oligonucleotides increased in the order 2-mer 3-mer 4-mer ? 7-mer. The rate constants for dinucleotide and trinucleotide formation are more than 1000 times larger than those measured in the absence of montmorillonite. The rate constants for the formation of dinucleotide, trinucleotide, and tetranucleotide are 41, 2.6, and 3.7 times larger than those for the formation of oligo(G)s with a poly(C) template. The hydrolysis of ImpA was accelerated 35 times in the presence of the montmorillonite. The catalytic ability of montmorillonite to form dinucleotides and oligonucleotides is quantitatively evaluated and possible pathways for oligo(A) formation are proposed.

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