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(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate

ALDRICH/535303 - 96%

Synonym: (3-Hydroxy-3H-1,2,3-triazolo[4,5-b]pyridinato-O)tri-1-pyrrolidinyl-phosphorus hexafluorophosphate; PyAOP

CAS Number: 156311-83-0
Empirical Formula (Hill Notation): C17H27F6N7OP2
Molecular Weight: 521.38
MDL Number: MFCD03703417
Linear Formula: C17H27F6N7OP2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-535303-1G 1 g
$117.00
1/EA
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45-535303-5G 5 g
$281.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 535303-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 535303-5G

 

application(s) peptide synthesis
assay 96%
InChI 1S/C17H27N7OP.F6P/c1-2-11-21(10-1)26(22-12-3-4-13-22,23-14-5-6-15-23)25-24-17-16(19-20-24)8-7-9-18-17;1-7(2,3,4,5)6/h7-9H,1-6,10-15H2;/q+1;-1
InChI key CBZAHNDHLWAZQC-UHFFFAOYSA-N
mp 163-168 °C (lit.)
Quality Level 100 
reaction suitability reaction type: Coupling Reactions
SMILES string F[P-](F)(F)(F)(F)F.C1CCN(C1)[P+](On2nnc3cccnc23)(N4CCCC4)N5CCCC5
storage temp. −20°C
Application: Reagent for synthesis of:
Cyclic RGC pentapeptides for functionalization through click chemistry
Fluorescent glucose bioprobes
ReactIR flow cell

Reagent for:
Disulfide bond engineering
Heteroaryl ether synthesis
Optimization of conformational constraint on non-phosphorylated cyclic peptide antagonists of the Grb2-SH2 domain
Legal Information: ReactIR is a trademark of Mettler-Toledo, Inc.
Legal Information: Sold under agreement with PE Biosystems
Packaging: 1, 5 g in poly bottle
Purity 96%
mp 163-168 °C (lit.)
Storage Temp. −20°C
UNSPSC 12352101

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