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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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)-

Pyrrolidinium, 1-(fluoro-1-pyrrolidinylmethylene)-,hexafluorophosphate(1-)

F[P+](F)(F)(F)(F)F.F[C+](N1CCCC1)N1CCCC1 Request for Quotation
Chemical Name: Pyrrolidinium, 1-(fluoro-1-pyrrolidinylmethylene)-,hexafluorophosphate(1-)
CAS Number: 164298-25-3
Product Number: AG001URB(AGN-PC-0Q8L8F)
Synonyms:
MDL No:
Molecular Formula: C9H16F7N2P++
Molecular Weight: 316.1993

Identification/Properties

Properties
MP:
154-160 °C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Stability:
Moisture Sensitive
Computed Properties
Molecular Weight:
316.204g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
1
Exact Mass:
316.094g/mol
Monoisotopic Mass:
316.094g/mol
Topological Polar Surface Area:
6.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
228
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3261
Hazard Statements:
H314-H318
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The Bis(tetramethylene)fluoroformamidinium hexafluorophosphate is a versatile chemical reagent commonly utilized in chemical synthesis processes. This compound serves as an efficient reagent for the transformation of various functional groups in organic molecules. Its unique properties make it particularly useful in the synthesis of complex compounds and in the modification of biomolecules.This reagent is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, playing a crucial role in the construction of diverse molecular structures. Additionally, Bis(tetramethylene)fluoroformamidinium hexafluorophosphate is known for its ability to facilitate challenging chemical reactions with high efficiency and selectivity.Furthermore, this compound finds extensive application in the field of medicinal chemistry for the synthesis of pharmaceutical intermediates and bioactive molecules. Its compatibility with a wide range of functional groups and its ability to promote various types of chemical transformations make it a valuable tool for synthetic chemists working in drug discovery and development.Overall, the Bis(tetramethylene)fluoroformamidinium hexafluorophosphate stands out as a versatile reagent that significantly enhances the efficiency and scope of chemical synthesis, enabling the rapid and precise assembly of complex molecular structures with diverse applications.