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Uridine 2'-S-(4-methoxyphenyl)-2'-thio- is a chemical compound with the molecular formula C14H18N2O6S. It is a modified nucleoside, derived from the natural nucleoside uridine, which is a component of RNA. The compound features a 2'-thio linkage with a 4-methoxyphenyl group attached to the sulfur atom, which distinguishes it from the parent compound. This modification can affect the compound's chemical properties and interactions with other molecules, potentially leading to different biological activities compared to uridine. The compound is of interest in chemical and biological research, particularly in the study of nucleic acid chemistry and the development of new therapeutic agents.

85207-45-0

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85207-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85207-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85207-45:
(7*8)+(6*5)+(5*2)+(4*0)+(3*7)+(2*4)+(1*5)=130
130 % 10 = 0
So 85207-45-0 is a valid CAS Registry Number.

85207-45-0SDS

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 1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-(4-methoxyphenyl)sulfanyloxolan-2-yl]pyrimidine-2,4-dione

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

1.5 Emergency phone number

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More Details:85207-45-0 SDS

85207-45-0Relevant academic research and scientific papers

Nucleic Acid Related Compounds. 73. Fluorination of Uridine 2'-Thioethers with Xenon Difluoride or (Diethylamino)sulfur Trifluoride. Synthesis of Stable 2'--2'-deoxy-2'-fluorouridines

Robins, Morris J.,Mullah, Khairuzzaman B.,Wnuk, Stanislaw F.,Dalley, N. Kent

, p. 2357 - 2364 (1992)

Treatment of 2,2'-anhydro-1-β-D-arabinofuranosyluracil with thiolate anions gave the 2'-S-alkyl(and aryl)-2'-thiouridines (1).Oxidation of 3',5'-di-O-acetyl-2'-S-alkyl(and aryl)-2'-thiouridines (2) with 3-chloroperoxybenzoic acid (MCPBA) gave the diastere

FACILE SYNTHESIS OF 2'-DEOXY-2'-ARYLTHIOURIDINES

Matsuda, Akira,Miyasaka, Tadashi

, p. 55 - 58 (2007/10/02)

Cleavage of the anhydro linkage of O2, 2'-cyclouridine (1a) with o-, m-, and p-substituted thiophenols and β-naphthalenethiol was carried out in dimethylformamide to give the corresponding 2'-deoxy-2'-arylthiouridines (6a-g) in good yields.

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