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5-(6-amino-2-chloro-purin-9-yl)-2-(hydroxymethyl)oxolan-3-ol, commonly known as cladribine, is a synthetic purine nucleoside analog characterized by its immunosuppressive and antineoplastic properties. It is a potent drug that interferes with DNA synthesis and repair, thereby disrupting cellular processes and leading to cell death. Cladribine is used in the treatment of various conditions, including hairy cell leukemia, multiple sclerosis, and certain autoimmune diseases, and is administered either orally or as a subcutaneous injection.

5542-92-7

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5542-92-7 Usage

Uses

Used in Oncology:
5-(6-amino-2-chloro-purin-9-yl)-2-(hydroxymethyl)oxolan-3-ol is used as an antineoplastic agent for the treatment of hairy cell leukemia. It targets and destroys cancer cells by inhibiting their ability to synthesize and repair DNA, thereby reducing disease activity and controlling symptoms in affected patients.
Used in Neurology:
In the field of neurology, 5-(6-amino-2-chloro-purin-9-yl)-2-(hydroxymethyl)oxolan-3-ol is used as an immunosuppressive agent for the treatment of multiple sclerosis. It helps to reduce inflammation and demyelination in the central nervous system, improving the quality of life for patients with this condition.
Used in Autoimmune Diseases:
5-(6-amino-2-chloro-purin-9-yl)-2-(hydroxymethyl)oxolan-3-ol is utilized as an immunosuppressive therapy for the management of certain autoimmune diseases. By dampening the immune response, it can help to alleviate symptoms and prevent further damage to the affected tissues.

Check Digit Verification of cas no

The CAS Registry Mumber 5542-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,4 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5542-92:
(6*5)+(5*5)+(4*4)+(3*2)+(2*9)+(1*2)=97
97 % 10 = 7
So 5542-92-7 is a valid CAS Registry Number.

5542-92-7SDS

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 5-(6-amino-2-chloropurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol

1.2 Other means of identification

Product number -
Other names 2CdA

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:5542-92-7 SDS

5542-92-7Downstream Products

5542-92-7Relevant academic research and scientific papers

Selective Preparations of Purine Nucleosides and Nucleotides: Reagents and Methods

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Paragraph 0151, (2016/04/06)

A process of regiospecific synthesis of N-9 purine nucleoside analogs in either solution or solid phase synthesis is described. The introduction of the sugar moiety or its analogue on to a 6-heteroarylium purine or its mesomeric betaine so that formation of only the N-9 position regioisomers of the purine nucleoside analogs (either D or L enantiomers) is obtained. This regiospecific introduction of the sugar moiety allows the synthesis of purine nucleoside analogs in high yields without formation of the N-7-positional regioisomers, while the 6-heteroaryliums are leaving groups facilitated for nucleophilic displacement. Solid supported 6-heterarylium purine bases can be used for purine based library synthesis and synthesis of nucleotide monophosphates and polyphosphates. Processes for providing novel 6-heteroarylium purines and their corresponding mesomeric betaines for the regiospecific synthesis of N-9 purine nucleoside analogs and nucleotides are described.

METHODS FOR SELECTIVE N-9 GLYCOSYLATION OF PURINES

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Page/Page column 61, (2010/11/25)

A process for providing regiospecific and highly stereoselective synthesis of 9-β anomeric purine nucleoside analogs is described. The introduction of the sugar moiety on to 6-(azolyl)-substituted purine bases is performed so that highly stereoselective formation of the β anomers of only the 9 position regioisomers of the purine nucleoside analogs (either D or L enantiomers) is obtained. This regiospecific and stereoselective introduction of the sugar moiety allows the synthesis of nucleoside analogs, and in particular 2'-deoxy, 3'-deoxy, 2'-deoxy-2'-halo-arabino and 2',3'-dideoxy-2'-halo-threo purine nucleoside analogs, in high yields without formation of the 7-positional regioisomers. Processes for providing novel 6-(azolyl)purines for the regiospecific and highly stereoselective synthesis of 9-β anomeric purine nucleoside analogs are described. The compounds are drugs or intermediates to drugs.

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