539899
Bis(pentafluorophenyl) carbonate
97%, for peptide synthesis
Synonym(s):
Pentafluorophenyl carbonate
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product name
Bis(pentafluorophenyl) carbonate, 97%
Quality Level
Assay
97%
reaction suitability
reaction type: Carbonylations
mp
47-50 °C (lit.)
application(s)
peptide synthesis
SMILES string
Fc1c(F)c(F)c(OC(=O)Oc2c(F)c(F)c(F)c(F)c2F)c(F)c1F
InChI
1S/C13F10O3/c14-1-3(16)7(20)11(8(21)4(1)17)25-13(24)26-12-9(22)5(18)2(15)6(19)10(12)23
InChI key
IOVVFSGCNWQFQT-UHFFFAOYSA-N
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General description
Bis(pentafluorophenyl) carbonate is the equivalent of carbonyl compound generally used in coupling reactions. It is used as a reagent in the preparation of azapeptides.
Application
Bis(pentafluorophenyl) carbonate can be used in the preparation of:
- A cyclic carbonate named 6,6′-(ethane-1,2-diyl)bis(1,3,6-dioxazocan-2-one), which is a key intermediate for the synthesis of non-isocyanate polyurethanes.
- A coumarin based aliphatic polycarbonate named 5-(4-methylumbelliferyloxycarbonyl)-5-methyl-1,3-dioxan-2-one (MUC).
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
230.0 °F - closed cup
Flash Point(C)
110 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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[Dipentafluorophenylcarbonate in the synthesis of oligonucleotides by the H-phosphonate method].
Bioorganicheskaia khimiia, 20(3), 323-326 (1994-03-01)
Bis(pentafluorophenyl)carbonate
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2004)
Dipentafluorophenyl carbonate--a reagent for the synthesis of oligonucleotides and their conjugates.
Nucleic acids research, 21(23), 5337-5344 (1993-11-25)
Dipentafluorophenyl carbonate has been successfully used as condensing agent for the internucleotide bond formation in the synthesis of oligonucleotides via H-phosphonate approach. The mechanism of a nucleotide component activation with this reagent has been investigated with the help of 31P
Bioorganicheskaia khimiia, 15(4), 460-464 (1989-04-01)
Dipentafluorophenylcarbonate, belonging to transesterifiying reagents, has been prepared and used for the synthesis of pentafluorophenyl esters of amino acids. In contrast to many other reagents of the kind, its preparation is simple, it is highly reactive and at the same
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