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[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-2-[[[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy-hydroxy-phosphoryl]oxymethyl]-4-hydroxy-oxolan-3-yl]oxyphosphonic acid is a nucleotide analog with a complex structure, consisting of a purine base (6-aminopurin-9-yl) linked to a sugar molecule (oxolan-3-yl) and a phosphonic acid molecule. [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-2-[[[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy-hydroxy-phosphoryl]oxymethyl]-4-hydroxy-oxolan-3-yl]oxyphosphonic acid is characterized by its specific molecular interactions and is valuable in the study of nucleic acid biochemistry and drug development.

3536-89-8

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3536-89-8 Usage

Uses

Used in Pharmaceutical Industry:
[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-2-[[[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy-hydroxy-phosphoryl]oxymethyl]-4-hydroxy-oxolan-3-yl]oxyphosphonic acid is used as a building block for nucleotide analogs in the development of antiviral and anticancer drugs. Its intricate structure allows for specific molecular interactions that can be exploited to target viral and cancerous cells, making it a promising candidate for therapeutic applications.
Used in Research and Development:
In the field of biochemistry, [(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-2-[[[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy-hydroxy-phosphoryl]oxymethyl]-4-hydroxy-oxolan-3-yl]oxyphosphonic acid serves as a valuable tool for studying the biochemistry of nucleic acids. Its unique properties and interactions can provide insights into the mechanisms of nucleic acid function and the development of new therapeutic strategies.
Used in Synthesis of Nucleic Acids:
[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-2-[[[(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy-hydroxy-phosphoryl]oxymethyl]-4-hydroxy-oxolan-3-yl]oxyphosphonic acid is also commonly used in the synthesis of nucleic acids, which are essential for various biological processes, including the storage and transmission of genetic information. Its role in nucleic acid synthesis highlights its importance in both basic research and the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 3536-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3536-89:
(6*3)+(5*5)+(4*3)+(3*6)+(2*8)+(1*9)=98
98 % 10 = 8
So 3536-89-8 is a valid CAS Registry Number.

3536-89-8SDS

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 (2S)-2-(3,4-dihydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one

1.2 Other means of identification

Product number -
Other names Isocoreopsin

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:3536-89-8 SDS

3536-89-8Upstream product

3536-89-8Downstream Products

3536-89-8Relevant academic research and scientific papers

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