MedKoo Cat#: 581693 | Name: Decafluorobiphenyl
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Decafluorobiphenyl is used as an intermediate in organic synthesis and in pharmaceuticals.

Chemical Structure

Decafluorobiphenyl
Decafluorobiphenyl
CAS#434-90-2

Theoretical Analysis

MedKoo Cat#: 581693

Name: Decafluorobiphenyl

CAS#: 434-90-2

Chemical Formula: C12F10

Exact Mass: 333.9840

Molecular Weight: 334.12

Elemental Analysis: C, 43.14; F, 56.86

Price and Availability

Size Price Availability Quantity
5g USD 250.00 2 Weeks
25g USD 550.00 2 Weeks
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Related CAS #
No Data
Synonym
Perfluorobiphenyl; Biphenyl, decafluoro-; Perfluorodiphenyl; Decafluorobiphenyl
IUPAC/Chemical Name
1,1'-Biphenyl, 2,2',3,3',4,4',5,5',6,6'-decafluoro-
InChi Key
ONUFSRWQCKNVSL-UHFFFAOYSA-N
InChi Code
InChI=1S/C12F10/c13-3-1(4(14)8(18)11(21)7(3)17)2-5(15)9(19)12(22)10(20)6(2)16
SMILES Code
FC1=C(C2=C(F)C(F)=C(F)C(F)=C2F)C(F)=C(F)C(F)=C1F
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 334.12 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Alapour S, de la Torre BG, Ramjugernath D, Koorbanally NA, Albericio F. Application of Decafluorobiphenyl (DFBP) Moiety as a Linker in Bioconjugation. Bioconjug Chem. 2018 Feb 21;29(2):225-233. doi: 10.1021/acs.bioconjchem.7b00800. Epub 2018 Jan 24. Review. PubMed PMID: 29341592. 2: Landmann J, Hennig PT, Ignat'ev NV, Finze M. Borylation of fluorinated arenes using the boron-centred nucleophile B(CN)(3)(2-) - a unique entry to aryltricyanoborates. Chem Sci. 2017 Sep 1;8(9):5962-5968. doi: 10.1039/c7sc02249b. Epub 2017 Jun 26. PubMed PMID: 28989626; PubMed Central PMCID: PMC5620525. 3: Ngambenjawong C, Pineda JM, Pun SH. Engineering an Affinity-Enhanced Peptide through Optimization of Cyclization Chemistry. Bioconjug Chem. 2016 Dec 21;27(12):2854-2862. doi: 10.1021/acs.bioconjchem.6b00502. Epub 2016 Nov 10. PubMed PMID: 27779387; PubMed Central PMCID: PMC5678939. 4: Ferrer M, Pedrosa A, Rodríguez L, Rossell O, Vilaseca M. New insights into the factors that govern the square/triangle equilibria of Pd(II) and Pt(II) supramolecules. Unexpected participation of a mononuclear species in the equilibrium. Inorg Chem. 2010 Oct 18;49(20):9438-49. doi: 10.1021/ic101150p. PubMed PMID: 20866091. 5: Mikami T, Miyatake K, Watanabe M. Poly(arylene ether)s containing superacid groups as proton exchange membranes. ACS Appl Mater Interfaces. 2010 Jun;2(6):1714-21. doi: 10.1021/am100224z. PubMed PMID: 20491452. 6: Schaub T, Fischer P, Steffen A, Braun T, Radius U, Mix A. C-F activation of fluorinated arenes using NHC-stabilized nickel(0) complexes: selectivity and mechanistic investigations. J Am Chem Soc. 2008 Jul 23;130(29):9304-17. doi: 10.1021/ja074640e. Epub 2008 Jun 28. PubMed PMID: 18588290. 7: Schaub T, Backes M, Radius U. Catalytic C-C bond formation accomplished by selective C-F activation of perfluorinated arenes. J Am Chem Soc. 2006 Dec 20;128(50):15964-5. PubMed PMID: 17165711. 8: Batsanov AS, Collings JC, Marder TB. Arene-perfluoroarene interactions in crystal engineering. XV. Ferrocene-decafluorobiphenyl (1/1). Acta Crystallogr C. 2006 Jun;62(Pt 6):m229-31. Epub 2006 May 16. PubMed PMID: 16763297. 9: Wang J, Cooper G, Tulumello D, Hitchcock AP. Inner shell excitation spectroscopy of biphenyl and substituted biphenyls: probing ring-ring delocalization. J Phys Chem A. 2005 Dec 8;109(48):10886-96. PubMed PMID: 16331932. 10: Matsumoto K, Ishizuka T, Harada T, Matsuoka H. Association behavior of fluorine-containing and non-fluorine-containing methacrylate-based amphiphilic diblock copolymer in aqueous media. Langmuir. 2004 Aug 17;20(17):7270-82. PubMed PMID: 15301515. 11: Arai T, Takasugi K, Esumi K. Mixed Micellar Properties of Nonionic Saccharide and Anionic Fluorocarbon Surfactants in Aqueous Solution. J Colloid Interface Sci. 1998 Jan 1;197(1):94-100. PubMed PMID: 9466848.