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CS-W001157 4
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3'-TBDMS-ibu-rG Phosphoramidite

  • CAS No. 1445905-51-0

  • Cat. No. CS-0158089
  • Purity≥97%
  • MDL No.MFCD30475539

*For research and further manufacturing use only, not for direct human use.

3'-TBDMS-ibu-rG Phosphoramidite|CS-0158089

Structure of 1445905-51-0

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General Information

  • CAS No. 1445905-51-0
  • Cat. No. CS-0158089
  • Purity ≥97%
  • MDL No. MFCD30475539
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅₀H₆₈N₇O₉PSi
  • Molecular Weight 970.18
  • Synonym(s) None
  • SMILES COC(C=C1)=CC=C1C(C2=CC=CC=C2)(C3=CC=C(OC)C=C3)OC[C@@H]4[C@@H](OP(N(C(C)C)C(C)C)OCCC#N)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N5C(N=C(NC(C(C)C)=O)NC6=O)=C6N=C5)O4

Description

3'-TBDMS-ibu-rG Phosphoramidite delivers a protected guanine building block with orthogonal functionality for solid-phase oligonucleotide synthesis. The TBDMS group at the 3' position provides robust protection against degradation, while the ibu (isobutyryl) moiety enhances stability and facilitates efficient coupling. This phosphoramidite integrates seamlessly into nucleic acid sequences under standard conditions, enabling precise incorporation of modified guanosine units in therapeutic and diagnostic applications.

Application

3'-TBDMS-ibu-rG phosphoramidite serves as a key building block for the synthesis of modified oligonucleotides, enabling site-specific incorporation of a 3'-O-(tert-butyldimethylsilyl)-protected inosine derivative. The TBDMS group provides robust protection during synthesis and facilitates selective deprotection under mild conditions. Its compatibility with standard solid-phase synthesis protocols and excellent stability make it ideal for constructing complex nucleic acid architectures requiring orthogonal functionalization.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   184.31
  • LogP   9.68898
  • H_Acceptors   14
  • H_Donors   2
  • Rotatable_Bonds   21

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