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Merck
CN

44629

2,6-Difluorophenyl pentafluorophenyl suberate

≥97.0% (HPLC)

Synonym(s):

2,6-Difluorophenyl pentafluorophenyl octanedioate, Octanedioic acid 1-(2,6-difluorophenyl) 8-(2,3,4,5,6-pentafluorophenyl) ester

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About This Item

Empirical Formula (Hill Notation):
C20H15F7O4
CAS Number:
1370727-01-7
Molecular Weight:
452.32
UNSPSC Code:
12352204
NACRES:
NA.25
PubChem Substance ID:
329756526
MDL number:
MFCD25977822
Beilstein/REAXYS Number:
22620423

Key Documents

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Product Name

2,6-Difluorophenyl pentafluorophenyl suberate, ≥97.0% (HPLC)

SMILES string

O=C(CCCCCCC(OC1=C(F)C=CC=C1F)=O)OC2=C(F)C(F)=C(F)C(F)=C2F

InChI key

QCEAIUJTXLLHIX-UHFFFAOYSA-N

InChI

1S/C20H15F7O4/c21-10-6-5-7-11(22)19(10)30-12(28)8-3-1-2-4-9-13(29)31-20-17(26)15(24)14(23)16(25)18(20)27/h5-7H,1-4,8-9H2

assay

≥97.0% (HPLC)

Quality Level

100

Application

This linker enables to form heteroconjugates by linking primary amino groups from two separate biomolecules in a strictly orthogonal way. The orthogonality arises from the differential reactivity of the ester leaving groups.

pictograms

Exclamation mark
GHS07

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

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBK9001V
BCBK9001

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Adam T Slósarczyk et al.
Journal of peptide science : an official publication of the European Peptide Society, 18(4), 261-269 (2012-03-07)
An efficient method for the heteroconjugation of biomolecules carrying free amino groups was reported previously, where mixed polyfluorophenyl diesters of dicarboxylic acids with varied aliphatic chain length were shown to be efficient reagents for the conjugation of a variety of

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