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5-[3-(TRIFLUOROACETAMIDO)-E-1-PROPENYL]-2'-DEOXYURIDINE is a chemical compound with the molecular formula C11H12F3N2O5. It is a modified nucleoside derivative that has potential applications in various fields due to its unique structure and properties.

115794-55-3

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115794-55-3 Usage

Uses

Used in Pharmaceutical Industry:
5-[3-(TRIFLUOROACETAMIDO)-E-1-PROPENYL]-2'-DEOXYURIDINE is used as a reactant/reagent for "Corey's reagent," which is 3,5-di-tert-butyl-1,2-benzoquinone. This reagent is essential in the synthesis of various pharmaceutical compounds, making it a valuable component in drug development.
Used in Chemical Synthesis:
In the field of chemical synthesis, 5-[3-(TRIFLUOROACETAMIDO)-E-1-PROPENYL]-2'-DEOXYURIDINE serves as a modifying agent. It is particularly useful in the synthesis of fluorescent and double-headed nucleosides, which have applications in molecular biology and biochemistry research.
These applications highlight the versatility of 5-[3-(TRIFLUOROACETAMIDO)-E-1-PROPENYL]-2'-DEOXYURIDINE in different industries, showcasing its potential as a valuable compound for various purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 115794-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,9 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 115794-55:
(8*1)+(7*1)+(6*5)+(5*7)+(4*9)+(3*4)+(2*5)+(1*5)=143
143 % 10 = 3
So 115794-55-3 is a valid CAS Registry Number.

115794-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3''-trifluoroacetamidoallyl)-2'-deoxyuridine

1.2 Other means of identification

Product number -
Other names 5-[3-(TRIFLUOROACETAMIDO)-E-1-PROPENYL]-2'-DEOXYURIDINE

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:115794-55-3 SDS

115794-55-3Relevant articles and documents

A cysteine-appended deoxyuridine for the postsynthetic DNA modification using native chemical ligation

Takeda, Shuji,Tsukiji, Shinya,Nagamune, Teruyuki

, p. 2235 - 2238 (2005)

A new deoxyuridine derivative 6 bearing a cysteine group at the C5 position was synthesized and incorporated into oligodeoxynucleotide (ODN) by phosphoramidite chemistry. The postsynthetic DNA modification of the cysteine-containing ODN using native chemi

Ketone-DNA: A versatile postsynthetic DNA decoration platform

Dey, Subhakar,Sheppard, Terry L.

, p. 3983 - 3986 (2001)

matrix presented A general strategy for the functional diversification of DNA oligonucleotides under physiological conditions was developed. We describe the synthesis of DNA molecules bearing ketone ports (ketone-DNA) and the efficient postsynthetic decor

Single-stranded labelled oligonucleotides, reactive monomers and methods of synthesis

-

, (2008/06/13)

Substantially pure single-stranded oligonucleotides having a preselected sequence of not more than about 200 nucleotides, at least one of which is at a preselected position in the sequence and includes a base with a covalently attached linker arm containing or capable of binding at least one reporter group or solid support. A process for the chemical synthesis of the substantially pure single-stranded oligonucleotide and modified nucleosides useful in such synthesis are provided.

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