N2-Phenoxyacetyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)guanosine

95%

Reagent Code: #51651
fingerprint
CAS Number 131474-72-1

science Other reagents with same CAS 131474-72-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 659.88 g/mol
Formula C₃₀H₄₅N₅O₈Si₂
badge Registry Numbers
MDL Number MFCD27976862
inventory_2 Storage & Handling
Density 1.32±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This chemical is primarily utilized in the field of nucleotide chemistry and oligonucleotide synthesis. It serves as a protected guanosine derivative, where the phenoxyacetyl group safeguards the exocyclic amine, and the tetraisopropyldisiloxane (TIPDS) group protects the 3' and 5' hydroxyls. This protection is crucial during the stepwise construction of oligonucleotides, particularly in solid-phase synthesis, ensuring selective reactivity and preventing unwanted side reactions. The compound is especially valuable in the synthesis of modified oligonucleotides for research applications, such as the development of antisense oligonucleotides, siRNAs, and other therapeutic nucleic acids. Its use enhances the efficiency and precision of nucleotide assembly, making it a key reagent in molecular biology and drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿1,692.00
inventory 50mg
10-20 days ฿6,480.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N2-Phenoxyacetyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)guanosine
No image available

This chemical is primarily utilized in the field of nucleotide chemistry and oligonucleotide synthesis. It serves as a protected guanosine derivative, where the phenoxyacetyl group safeguards the exocyclic amine, and the tetraisopropyldisiloxane (TIPDS) group protects the 3' and 5' hydroxyls. This protection is crucial during the stepwise construction of oligonucleotides, particularly in solid-phase synthesis, ensuring selective reactivity and preventing unwanted side reactions. The compound is especiall

This chemical is primarily utilized in the field of nucleotide chemistry and oligonucleotide synthesis. It serves as a protected guanosine derivative, where the phenoxyacetyl group safeguards the exocyclic amine, and the tetraisopropyldisiloxane (TIPDS) group protects the 3' and 5' hydroxyls. This protection is crucial during the stepwise construction of oligonucleotides, particularly in solid-phase synthesis, ensuring selective reactivity and preventing unwanted side reactions. The compound is especially valuable in the synthesis of modified oligonucleotides for research applications, such as the development of antisense oligonucleotides, siRNAs, and other therapeutic nucleic acids. Its use enhances the efficiency and precision of nucleotide assembly, making it a key reagent in molecular biology and drug discovery.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...