N6,3'-O-Dibenzoyl-2'-deoxyadenosine
97%
- Product Code: 109047
CAS:
51549-54-3
Molecular Weight: | 459.45 g./mol | Molecular Formula: | C₂₄H₂₁N₅O₅ |
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EC Number: | MDL Number: | MFCD00056180 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of biochemical research, particularly in the study of nucleic acids and their derivatives. It serves as a protected form of deoxyadenosine, where the benzoyl groups shield the reactive sites, allowing for controlled synthesis and modification of oligonucleotides. This compound is often employed in the development of nucleoside analogs, which are crucial in exploring potential therapeutic agents, especially in antiviral and anticancer drug research. Additionally, it plays a role in the synthesis of modified DNA sequences for various molecular biology applications, including gene editing and the study of DNA-protein interactions. Its use ensures precise and efficient incorporation of modified nucleosides into DNA strands, aiding in the advancement of genetic and pharmaceutical studies.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.010 | 10-20 days | ฿12,600.00 |
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N6,3'-O-Dibenzoyl-2'-deoxyadenosine
This chemical is primarily utilized in the field of biochemical research, particularly in the study of nucleic acids and their derivatives. It serves as a protected form of deoxyadenosine, where the benzoyl groups shield the reactive sites, allowing for controlled synthesis and modification of oligonucleotides. This compound is often employed in the development of nucleoside analogs, which are crucial in exploring potential therapeutic agents, especially in antiviral and anticancer drug research. Additionally, it plays a role in the synthesis of modified DNA sequences for various molecular biology applications, including gene editing and the study of DNA-protein interactions. Its use ensures precise and efficient incorporation of modified nucleosides into DNA strands, aiding in the advancement of genetic and pharmaceutical studies.
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