N2-Phenylacetyl Guanosine

≥98%

Reagent Code: #97313
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CAS Number 132628-16-1

science Other reagents with same CAS 132628-16-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 401.37 g/mol
Formula C₁₈H₁₉N₅O₆
thermostat Physical Properties
Melting Point 189 °C
inventory_2 Storage & Handling
Density 1.73g/mL
Storage room temperature, dry

description Product Description

N2-Phenylacetyl Guanosine is a protected form of guanosine commonly used as a building block in the chemical synthesis of RNA oligonucleotides. The phenylacetyl group serves as a protecting group for the N2 amino position of the guanine base, preventing unwanted side reactions during solid-phase synthesis. It is essential in biochemical research for producing modified RNA molecules to study nucleic acid structure, function, and modifications. This compound facilitates the exploration of gene expression, RNA-protein interactions, and RNA processing mechanisms. Additionally, it supports the development of therapeutic oligonucleotides targeting RNA-related diseases.

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inventory 5g
10-20 days ฿3,231.00

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N2-Phenylacetyl Guanosine
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N2-Phenylacetyl Guanosine is a protected form of guanosine commonly used as a building block in the chemical synthesis of RNA oligonucleotides. The phenylacetyl group serves as a protecting group for the N2 amino position of the guanine base, preventing unwanted side reactions during solid-phase synthesis. It is essential in biochemical research for producing modified RNA molecules to study nucleic acid structure, function, and modifications. This compound facilitates the exploration of gene expression,

N2-Phenylacetyl Guanosine is a protected form of guanosine commonly used as a building block in the chemical synthesis of RNA oligonucleotides. The phenylacetyl group serves as a protecting group for the N2 amino position of the guanine base, preventing unwanted side reactions during solid-phase synthesis. It is essential in biochemical research for producing modified RNA molecules to study nucleic acid structure, function, and modifications. This compound facilitates the exploration of gene expression, RNA-protein interactions, and RNA processing mechanisms. Additionally, it supports the development of therapeutic oligonucleotides targeting RNA-related diseases.

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