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72209-27-9

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  • high purity (2S,3S,4R,5R)-N-ethyl-3,4-dihydroxy-5-(1-hydroxy-6-imino-purin-9-yl)ox olane-2-carboxamide CAS NO.72209-27-9 CAS NO.72209-27-9

    Cas No: 72209-27-9

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72209-27-9 Usage

General Description

The chemicals "(2S,3S,4R,5R)-N-ethyl-3,4-dihydroxy-5-(1-hydroxy-6-imino-purin-9-yl)oxolane-2-carboxamide" is a complex compound with a molecular structure that includes a purine ring. It contains an N-ethyl group, as well as multiple hydroxyl groups, which gives it acidic properties. (2S,3S,4R,5R)-N-ethyl-3,4-dihydroxy-5-(1-hydroxy-6-imino-purin-9-yl)ox olane-2-carboxamide is categorized as a nucleoside derivative, and it bears similarity to adenosine and other purine-containing molecules. It may have potential biological activities related to its interaction with purine receptors or involvement in cellular signaling pathways. Its precise function and effects would need to be further studied and characterized in order to fully understand its significance in the context of biological and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 72209-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,0 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 72209-27:
(7*7)+(6*2)+(5*2)+(4*0)+(3*9)+(2*2)+(1*7)=109
109 % 10 = 9
So 72209-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N6O5/c1-2-14-11(21)8-6(19)7(20)12(23-8)17-3-15-5-9(13)18(22)4-16-10(5)17/h3-4,6-8,12-13,19-20,22H,2H2,1H3,(H,14,21)/b13-9-/t6-,7+,8-,12+/m0/s1

72209-27-9SDS

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 (2S,3S,4R,5R)-N-ethyl-3,4-dihydroxy-5-(1-hydroxy-6-iminopurin-9-yl)oxolane-2-carboxamide

1.2 Other means of identification

Product number -
Other names 1-(6-Amino-9H-purin-9-yl)-1-deoxy-N-ethylribofuranuronamide N-oxide

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

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

More Details:72209-27-9 SDS

72209-27-9Downstream Products

72209-27-9Relevant articles and documents

Ring opening reactions: Synthesis of AICAR analogs as potential antimetabolite agents

Costanzi,Lambertucci,Portino,Volpini,Vittori,Cristalli

, p. 415 - 418 (2005)

In an attempt to improve the A2A selectivity of the 2-(aryl)alkylthio derivatives of adenosine, we planned the synthesis of the corresponding derivatives of the 5′-N-ethylcarboxamidoadenosine (NECA). For this purpose, we designed the synthesis of 2-mercapto-NECA to be pursued by means of an opening-closure method. We obtained the open AICAR analog; however, ring closure efforts failed to give the desired compound. The newly synthesized AICAR derivative could potentially be endowed with antiviral or antitumoral activity. Copyright Taylor & Francis, Inc.

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