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Merck
CN

535303

(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate

96%, for peptide synthesis

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C17H27F6N7OP2
CAS Number:
Molecular Weight:
521.38
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22
MDL number:
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Product Name

(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate, 96%

Quality Segment

assay

96%

form

powder

reaction suitability

reaction type: Coupling Reactions

mp

163-168 °C (lit.)

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

F[P-](F)(F)(F)(F)F.C1CCN(C1)[P+](On2nnc3cccnc23)(N4CCCC4)N5CCCC5

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

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

Sold under agreement with PE Biosystems
ReactIR is a trademark of Mettler-Toledo, Inc.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves



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