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156311-83-0

Phosphorus(1+), [3-(hydroxy-κO)-3H-1,2,3-triazolo[4,5-b]pyridinato]tri-1-pyrrolidinyl-, (T-4)-, hexafluorophosphate(1-) (1:1)

Catalog#: AR001PDS  |   CAS#: 156311-83-0  |   MDL#: MFCD03703417  |   MF: C17H27F6N7OP2  |   MW: 521.3805

Packsize Purity Price Availability Quantity
1g 96% $4.00 Global Stock Buy Now Add To Cart
5g 96% $8.00 Global Stock Buy Now Add To Cart
10g 96% $13.00 Global Stock Buy Now Add To Cart
25g 96% $26.00 Global Stock Buy Now Add To Cart
50g 96% $52.00 Global Stock Buy Now Add To Cart
75g 96% $77.00 Global Stock Buy Now Add To Cart
100g 96% $87.00 Global Stock Buy Now Add To Cart
250g 96% $208.00 Global Stock Buy Now Add To Cart
500g 96% $347.00 Global Stock Buy Now Add To Cart
1000g 96% $661.00 Global Stock Buy Now Add To Cart
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Catalog Number AR001PDS
Chemical Name Phosphorus(1+), [3-(hydroxy-κO)-3H-1,2,3-triazolo[4,5-b]pyridinato]tri-1-pyrrolidinyl-, (T-4)-, hexafluorophosphate(1-) (1:1)
CAS Number 156311-83-0
Molecular Formula C17H27F6N7OP2
Molecular Weight 521.3805
MDL Number MFCD03703417
SMILES C1CCN(C1)[P+](N1CCCC1)(N1CCCC1)On1nnc2c1nccc2.F[P-](F)(F)(F)(F)F

[(7-Azabenzotriazol-1-yl)oxy]tris(pyrrolidino)phosphonium hexafluorophosphate, commonly referred to as $name$, is a versatile reagent widely utilized in chemical synthesis. This compound plays a crucial role as a highly efficient coupling agent in various organic reactions, particularly in peptide and nucleotide synthesis. $name$ is known for its ability to facilitate the formation of peptide bonds by activating carboxylic acids, enabling the coupling of amino acids to construct complex peptide chains. Its unique structure allows for rapid and high-yielding peptide bond formation, making it an essential tool in the field of pharmaceutical research and biochemistry.Additionally, $name$ is commonly employed in the synthesis of oligonucleotides, where it mediates the coupling of nucleotide phosphoramidites to construct DNA and RNA sequences. Its effectiveness in promoting phosphoramidite activation and coupling reactions makes it a valuable reagent in oligonucleotide synthesis, particularly in the development of nucleic acid-based therapeutics and molecular biology research.Overall, the application of $name$ in chemical synthesis extends beyond peptide and nucleotide synthesis, showcasing its versatility and importance in modern organic chemistry.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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