44629
2,6-Difluorophenyl pentafluorophenyl suberate
≥97.0% (HPLC)
别名:
2,6-Difluorophenyl pentafluorophenyl octanedioate, Octanedioic acid 1-(2,6-difluorophenyl) 8-(2,3,4,5,6-pentafluorophenyl) ester
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关于此项目
经验公式（希尔记法）:
C20H15F7O4
化学文摘社编号:
分子量:
452.32
UNSPSC Code:
12352204
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
22620423
产品名称
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
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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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