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1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-(hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione is a complex organic compound characterized by a cyclopentyl ring and a pyrimidinedione core. It features a fluorine atom and a hydroxymethyl group attached to the cyclopentyl ring, along with an iodine atom on the pyrimidinedione core. 1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)-5-iodo2,4(1H,3H)-pyrimidinedione is likely to possess significant biological activity, making it a potential candidate for pharmaceutical development or as a research tool in chemical biology. Its specific functions and potential applications would be contingent upon its properties and interactions within biological systems.

110864-93-2

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110864-93-2 Usage

Uses

Used in Pharmaceutical Development:
1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-(hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione is used as a potential pharmaceutical compound for its possible biological activity. 1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)-5-iodo2,4(1H,3H)-pyrimidinedione's unique structure, including the fluorine and iodine atoms, may allow it to interact with biological targets in ways that could be harnessed for therapeutic purposes.
Used in Chemical Biology Research:
In the field of chemical biology, 1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-(hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione serves as a research tool to investigate its interactions with various biological molecules. Understanding these interactions can provide insights into the compound's mode of action and its potential applications in developing new drugs or therapies.
Used in Drug Delivery Systems:
Similar to other bioactive compounds, 1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-(hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione may be employed in the development of drug delivery systems. These systems could be designed to improve the compound's bioavailability, targeting, and overall therapeutic efficacy.
Used in Anticancer Applications:
If the compound demonstrates anticancer properties, it could be used as an anticancer agent, targeting various types of cancer cells. Its specific mode of action would depend on its interactions with cancer-related biological pathways, potentially leading to the inhibition of tumor growth and progression.
Used in Diagnostic Applications:
1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)-5-iodo2,4(1H,3H)-pyrimidinedione's unique structure and potential biological activity may also make it useful in diagnostic applications, where it could be employed as a marker or imaging agent to detect or monitor certain diseases or conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 110864-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110864-93:
(8*1)+(7*1)+(6*0)+(5*8)+(4*6)+(3*4)+(2*9)+(1*3)=112
112 % 10 = 2
So 110864-93-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12FIN2O4/c11-7-6(1-4(3-15)8(7)16)14-2-5(12)9(17)13-10(14)18/h2,4,6-8,15-16H,1,3H2,(H,13,17,18)

110864-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-fluoro-3-hydroxy-4-(hydroxymethyl)cyclopentyl]-5-iodopyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-((1,2,3,4)-2-Fluoro-3-hydroxy-4-( hydroxymethyl)cyclopentyl)-5-iodo-2,4(1H,3H)-pyrimidinedione

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:110864-93-2 SDS

110864-93-2Downstream Products

110864-93-2Relevant academic research and scientific papers

Fluoro carbocyclic nucleosides: Synthesis and antiviral activity of 2'- and 6'-fluoro carbocyclic pyrimidine nucleosides including carbocyclic 1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-methyluracil and carbocyclic 1-(2-deoxy-2-fluoro-β-D-arabinofuranosy

Borthwick,Evans,Kirk,Biggadike,Exall,Youds,Roberts,Knight,Coates

, p. 179 - 186 (2007/10/02)

The racemic carbocyclic 2'-fluoroarabinosyl pyrimidine nucleosides 8, 9 (C-FIAU), 12, and 13 (C-FMAU) and the 2'-fluororibosyl pyrimidine nucleosides 17, 20, and 21 were prepared from their respective protected 2'-fluoro amino diols 5 and 14. The carbocyc

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