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154110-40-4

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154110-40-4 Usage

Description

(2R,3S,5R)-5-(4-ACETAMIDO-2-OXOPYRIMIDIN-1(2H)-YL)-2-((BIS(4-METHOXYPHENYL)(PHENYL)METHOXY)METHYL)TETRAHYDROFURAN-3-YL 2-CYANOETHYL DIISOPROPYLPHOSPHORAMIDITE is a complex organic compound with a unique molecular structure. It is characterized by its chiral centers at the 2nd, 3rd, and 5th positions, and its structure includes a tetrahydrofuran ring, a cyanoethyl group, and a diisopropylphosphoramidite moiety. (2R,3S,5R)-5-(4-ACETAMIDO-2-OXOPYRIMIDIN-1(2H)-YL)-2-((BIS(4-METHOXYPHENYL)(PHENYL)METHOXY)METHYL)TETRAHYDROFURAN-3-YL 2-CYANOETHYL DIISOPROPYLPHOSPHORAMIDITE is likely to have specific applications in various fields due to its unique chemical properties and reactivity.

Uses

Used in Pharmaceutical Industry:
(2R,3S,5R)-5-(4-ACETAMIDO-2-OXOPYRIMIDIN-1(2H)-YL)-2-((BIS(4-METHOXYPHENYL)(PHENYL)METHOXY)METHYL)TETRAHYDROFURAN-3-YL 2-CYANOETHYL DIISOPROPYLPHOSPHORAMIDITE is used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting nucleic acid-based therapies. Its unique structure allows for the formation of specific interactions with biological targets, making it a valuable component in the development of novel drugs.
Used in Chemical Research:
In the field of chemical research, this compound serves as a valuable tool for studying the properties and reactivity of complex organic molecules. Its unique structure can be used to investigate various chemical reactions and mechanisms, contributing to the advancement of synthetic chemistry and the development of new materials.
Used in Material Science:
(2R,3S,5R)-5-(4-ACETAMIDO-2-OXOPYRIMIDIN-1(2H)-YL)-2-((BIS(4-METHOXYPHENYL)(PHENYL)METHOXY)METHYL)TETRAHYDROFURAN-3-YL 2-CYANOETHYL DIISOPROPYLPHOSPHORAMIDITE may also find applications in material science, particularly in the development of new materials with specific properties. Its unique molecular structure could be utilized to create materials with tailored characteristics, such as improved stability, reactivity, or selectivity.
Used in Supramolecular Chemistry:
In supramolecular chemistry, this compound can be used as a building block for the construction of complex molecular assemblies. Its unique structure and functional groups can facilitate the formation of non-covalent interactions, such as hydrogen bonding and π-π stacking, leading to the development of supramolecular systems with specific functions and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 154110-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,1,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 154110-40:
(8*1)+(7*5)+(6*4)+(5*1)+(4*1)+(3*0)+(2*4)+(1*0)=84
84 % 10 = 4
So 154110-40-4 is a valid CAS Registry Number.

154110-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name DMT-dC(ac) Phosphoramidite

1.2 Other means of identification

Product number -
Other names Ac-dCPhosphoramidite

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:154110-40-4 SDS

154110-40-4Relevant articles and documents

Ultrafast cleavage and deprotection of oligonucleotides synthesis and use of C(Ac) derivatives

Reddy,Hanna, Naeem B.,Farooqui, Firdous

, p. 1589 - 1598 (2007/10/03)

We have investigated the use of alkylamines as fast cleavage and deprotection reagents for the solid phase synthesis of oligonucleotides and found methylamine/ammonium hydroxide (or methylamine) as an efficient reagent. The transamination side product formed with the commonly used dC(b2) has been eliminated by the use of dC(Ac) phosphoramidite. This system has successfully been used in the synthesis of oligonucleotides and oligonucleoside phosphorothioates. DMT dC(Ac) hydrogen phosphonate and DMT ribo C(Ac)-2'-OMe phosphoramidite also have been prepared and used in the synthesis of oligonucleotides.

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