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5'-O-[Bis(4-methoxyphenyl)phenylmethyl]cytidine is a chemically modified nucleoside derived from cytidine, a component of RNA. This modification involves the attachment of a bis(4-methoxyphenyl)phenylmethyl group at the 5' position of the ribose ring, which can significantly alter the compound's chemical and physical properties. This alteration may influence its interactions and functions within biological systems, making it a valuable candidate for research and medical applications focused on RNA structure, function, and related disease mechanisms.

112897-99-1

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112897-99-1 Usage

Uses

Used in Research Applications:
5'-O-[Bis(4-methoxyphenyl)phenylmethyl]cytidine is used as a research tool for studying the effects of nucleoside modifications on RNA structure and function. Its unique chemical properties allow scientists to investigate the role of modified nucleosides in various biological processes and their potential impact on RNA stability and activity.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]cytidine is used as a starting material or a molecular probe in the development of new drugs and therapies. Its potential to modulate RNA function makes it a candidate for treating diseases associated with RNA dysregulation, such as certain types of cancer and genetic disorders.
Used in Diagnostic Tools:
5'-O-[Bis(4-methoxyphenyl)phenylmethyl]cytidine may also be utilized in the creation of diagnostic tools that rely on the detection or manipulation of RNA molecules. Its distinctive chemical characteristics can be harnessed to improve the specificity and sensitivity of such tools, aiding in the early identification and monitoring of diseases related to RNA abnormalities.
Used in Drug Delivery Systems:
To enhance the bioavailability and therapeutic efficacy of 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]cytidine, it can be incorporated into drug delivery systems. These systems may include nanoparticles or other carriers designed to protect the compound, facilitate its transport across biological barriers, and ensure its targeted delivery to specific cells or tissues.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]cytidine serves as a building block or intermediate in the synthesis of more complex molecules with potential applications in medicine, materials science, and other areas. Its unique structure and reactivity make it a valuable component in the development of novel compounds with tailored properties.

Check Digit Verification of cas no

The CAS Registry Mumber 112897-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,9 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112897-99:
(8*1)+(7*1)+(6*2)+(5*8)+(4*9)+(3*7)+(2*9)+(1*9)=151
151 % 10 = 1
So 112897-99-1 is a valid CAS Registry Number.

112897-99-1SDS

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 5'-O-[Bis(4-methoxyphenyl)(phenyl)methyl]cytidine

1.2 Other means of identification

Product number -
Other names 5'-O-(4,4'-dimethoxytrityl)-cytidine

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:112897-99-1 SDS

112897-99-1Relevant academic research and scientific papers

1-(2,3-anhydro-β-D-lyxofuranosyl)cytosine derivatives as potential inhibitors of the human immunodeficiency virus

Webb,Mitsuya,Broder

, p. 1475 - 1479 (2007/10/02)

We report here that 1-(2,3-anhydro-β-D-lyxofuranosyl)cytosine has activity against the human immunodeficiency virus in vitro. A number of 2',3'-anhydro-β-D-lyxofuranosyl nucleoside derivatives were prepared, but none had the activity of the title compound. New efficient procedures were developed for the synthesis of 3'-deoxy-3'-alkyl- and 3'-deoxy-β-D-arabinosylpyrimidine derivatives.

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