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61671-80-5

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61671-80-5 Usage

Description

5-FLUORO-2'-O-METHYLURIDINE, also known as 5-FMU, is a modified nucleoside with a fluorine atom at the 5th position and a methyl group at the 2'-O position of the uridine molecule. It is a synthetic compound that has been studied for its potential applications in various fields, particularly in the pharmaceutical and biotechnology industries.

Uses

Used in Pharmaceutical Industry:
5-FLUORO-2'-O-METHYLURIDINE is used as an antineoplastic agent for the treatment of Ehrlich ascites carcinoma cells. It functions by inhibiting cell proliferation, which is a critical process in the growth and spread of cancer cells. 5-FLUORO-2'-O-METHYLURIDINE has shown promise in targeting and reducing the viability of cancer cells, making it a potential candidate for further research and development in cancer therapy.

Check Digit Verification of cas no

The CAS Registry Mumber 61671-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,7 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61671-80:
(7*6)+(6*1)+(5*6)+(4*7)+(3*1)+(2*8)+(1*0)=125
125 % 10 = 5
So 61671-80-5 is a valid CAS Registry Number.

61671-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluoro-1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-fluoro-O2'-methyl-uridine

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:61671-80-5 SDS

61671-80-5Downstream Products

61671-80-5Relevant articles and documents

General preparative synthesis of 2'-O-methylpyrimidine ribonucleosides

Ross,Springer,Vasquez,Andrews,Cook,Acevedo

, p. 765 - 769 (2007/10/02)

A convergent and general approach to synthesizing 2'-O-methylpyrimidine ribonucleosides 4a-e-, 6, 7 on a multigram scale is described which begins with an improved procedure for making larger quantities of 2-O-methyl-1,3,5-tri-O-benzoyl-α-D-ribose. The sugar was reacted with the desired silylated pyrimidines at room temperature under Vorbruggen conditions. The crude products contained less than 10% of the α anomers and the desired β anomers were isolated by crystallization. The blocked nucleosides were then deprotected and isolated by standard methods.

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