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Key Documents

Altri documenti

535303

Sigma-Aldrich

(7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate

96%, for peptide synthesis

Sinonimo/i:

(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

Formula empirica (notazione di Hill):
C17H27F6N7OP2
Numero CAS:
156311-83-0
Peso molecolare:
521.38
Numero MDL:
MFCD03703417
Codice UNSPSC:
12352101
ID PubChem:
329757954
NACRES:
NA.22

product name

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

Saggio

96%

Impiego in reazioni chimiche

reaction type: Coupling Reactions

Punto di fusione

163-168 °C (lit.)

applicazioni

peptide synthesis

Temperatura di conservazione

−20°C

Stringa SMILE

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
CBZAHNDHLWAZQC-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

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

Note legali

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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Zhaoguan Wu et al.
Scientific reports, 7, 46206-46206 (2017-04-08)
O-Acetylation of sialic acid in protein N-glycans is an important modification and can occur at either 4-, 7-, 8- or 9-position in various combinations. This modification is usually labile under alkaline reaction conditions. Consequently, a permethylation-based analytical method, which has
Si Liu et al.
Journal of proteomics, 181, 225-237 (2018-04-27)
Colorectal cancer (CRC) has become one of the most common cancers worldwide and the fifth most prevalent cancer in China with an upward trend in incidence rates. Altered glycosylation significantly affects the structural and functional changes in immunoglobulin G (IgG)
Yike Wu et al.
Analytical and bioanalytical chemistry, 409(16), 4027-4036 (2017-04-19)
A rapid and sensitive N-glycan profiling strategy for MALDI-MS incorporating the use of deglycosylation with microwave assistance and the co-derivatization of glycosylamine labeling with tris(2,4,6-trimethoxyphenyl)phosphonium acetic acid N-hydroxysuccinimide ester (TMPP-Ac-OSu) and methylamidation has been developed in this work. Notably, highly
Chang Wang et al.
Analytica chimica acta, 1002, 50-61 (2018-01-08)
Quantitative analysis of glycans is an emerging field in glycomic research. Herein we present a rapid and effective dual-labeling strategy, in the combination of isotopic derivatization of N-glycosylamine-based glycans by d0/d5-benzoyl chloride and methylamidation of sialic acids, to relatively quantify
Tarshona Stevens et al.
International journal of medicinal chemistry, 2012, 730239-730239 (2012-01-01)
The purpose of this study is to understand the interactions of some antibacterial cationic amphipathic cyclooctapeptides with calcium(II) and their secondary structural preferences. The thermodynamic parameters associated with calcium(II) interactions, between the antibacterial active cyclooctapeptides (COP 1-6) and those that
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