perfluorophenyl3-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)propanoate|1807530-07-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

perfluorophenyl3-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)propanoate

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Chemical Name:	perfluorophenyl3-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)propanoate
CAS Number:	1807530-07-9
Product Number:	AG00I087(AGN-PC-0WAM7P)
Synonyms:
MDL No:	MFCD26793779
Molecular Formula:
Molecular Weight:

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

413.301g/mol

XLogP3:

2.6

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

413.101g/mol

Monoisotopic Mass:

413.101g/mol

Topological Polar Surface Area:

68.4A^2

Heavy Atom Count:

Formal Charge:

Complexity:

499

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure

The Propanoic acid, 3-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]-, 2,3,4,5,6-pentafluorophenyl ester is a versatile compound utilized in chemical synthesis for the functionalization of various molecules. This compound acts as a valuable reagent in organic chemistry reactions, particularly in the modification of biomolecules and polymers. Its unique structure allows for selective and efficient derivatization of target compounds, enabling the introduction of specific functional groups or tags for further manipulation or characterization. This ester derivative plays a crucial role in the development of new materials, pharmaceuticals, and biologically active compounds through controlled chemical transformations.