5'-O-Trityl-N4-benzoyl-2'-deoxycytidine

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Reagent Code: #47946
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CAS Number 105862-10-0

science Other reagents with same CAS 105862-10-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 573.64 g/mol
Formula C₃₅H₃₁N₃O₅
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily used in the synthesis of oligonucleotides, particularly in the field of molecular biology and genetic research. It serves as a protected form of deoxycytidine, where the trityl group protects the 5'-hydroxyl and the benzoyl group protects the N4-amino group during the chemical synthesis of DNA strands. This protection is crucial for ensuring that the reactions occur selectively at the desired positions without unwanted side reactions. After the synthesis, these protecting groups can be removed to yield the desired oligonucleotide sequence. This compound is especially valuable in the production of modified nucleosides and nucleotides, which are essential for studies involving DNA sequencing, gene therapy, and the development of antisense oligonucleotides. Its application is critical in advancing research in genetics, biotechnology, and pharmaceutical development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,400.00
inventory 25mg
10-20 days ฿4,680.00

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5'-O-Trityl-N4-benzoyl-2'-deoxycytidine
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This chemical is primarily used in the synthesis of oligonucleotides, particularly in the field of molecular biology and genetic research. It serves as a protected form of deoxycytidine, where the trityl group protects the 5'-hydroxyl and the benzoyl group protects the N4-amino group during the chemical synthesis of DNA strands. This protection is crucial for ensuring that the reactions occur selectively at the desired positions without unwanted side reactions. After the synthesis, these protecting group

This chemical is primarily used in the synthesis of oligonucleotides, particularly in the field of molecular biology and genetic research. It serves as a protected form of deoxycytidine, where the trityl group protects the 5'-hydroxyl and the benzoyl group protects the N4-amino group during the chemical synthesis of DNA strands. This protection is crucial for ensuring that the reactions occur selectively at the desired positions without unwanted side reactions. After the synthesis, these protecting groups can be removed to yield the desired oligonucleotide sequence. This compound is especially valuable in the production of modified nucleosides and nucleotides, which are essential for studies involving DNA sequencing, gene therapy, and the development of antisense oligonucleotides. Its application is critical in advancing research in genetics, biotechnology, and pharmaceutical development.

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