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86480-42-4

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  • 2-(5-amino-3-methylsulfanyl-2,4,7,8,9-pentazabicyclo[4.3.0]nona-2,4,6,9-tetraen-8-yl)-5-(hydroxymethyl)oxolane-3,4-diol

    Cas No: 86480-42-4

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  • 2-(5-amino-3-methylsulfanyl-2,4,7,8,9-pentazabicyclo[4.3.0]nona-2,4,6,9-tetraen-8-yl)-5-(hydroxymethyl)oxolane-3,4-diol cas 86480-42-4

    Cas No: 86480-42-4

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86480-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86480-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,8 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86480-42:
(7*8)+(6*6)+(5*4)+(4*8)+(3*0)+(2*4)+(1*2)=154
154 % 10 = 4
So 86480-42-4 is a valid CAS Registry Number.

86480-42-4SDS

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 2-(7-amino-5-methylsulfanyltriazolo[4,5-d]pyrimidin-2-yl)-5-(hydroxymethyl)oxolane-3,4-diol

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

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More Details:86480-42-4 SDS

86480-42-4Downstream Products

86480-42-4Relevant articles and documents

Synthesis and Biological Evaluation of 2-Fluoro-8-azaadenosine and Related Compounds

Montgomery, John A.,Shortnacy, Anita T.,Secrist, John A.

, p. 1483 - 1489 (2007/10/02)

The synthesis of 2-fluoro-8-azaadenosine (6e) and 2-amino-8-azaadenosine (6d) is described.Condensation of 9H-2,6-bis(methylthio)-8-azapurine (4) with 2,3,5-tri-O-acetyl-D-ribofuranosyl chloride (5) produces a mixture of 6a (9-β-D-ribofuranosyl) and 7a (8-β-D-ribofuranosyl).Standard functional group manipulation, including a modified Schiemann reaction to introduce the fluorine, allows preparation of 6d and 6e from the major isomer 6a.By a similar series of reactions the minor component 7a was converted to 7d and 7e, with the ribose ring attached at N-8 of the 8-azapurine ring system.Structure proofs utilized UV and 1H and 13C NMR data.Compounds 6b-e,g and 7b-f were evaluated in the H.Ep.-2 cell culture screen, and compounds 6c-e and 7d were evaluated in the P388 mouse leukemia screen.Adenosine deaminase data are also presented for some compounds.

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