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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)-

1,4-Piperidinedicarboxylic acid, 4-fluoro-, 1-(1,1-dimethylethyl) ester

O=C(N1CCC(CC1)(F)C(=O)O)OC(C)(C)C Request for Quotation
Chemical Name: 1,4-Piperidinedicarboxylic acid, 4-fluoro-, 1-(1,1-dimethylethyl) ester
CAS Number: 614731-04-3
Product Number: AG003E1X(AGN-PC-056LK0)
Synonyms:
MDL No:
Molecular Formula: C11H18FNO4
Molecular Weight: 247.2633

Identification/Properties

Properties
BP:
346.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
247.266g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
247.122g/mol
Monoisotopic Mass:
247.122g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
316
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Boc-4-fluoropiperidine-4-carboxylic acid is a versatile chemical compound used extensively in organic synthesis. It serves as a crucial building block in the development of various pharmaceuticals, agrochemicals, and materials science products. Due to its unique structure, this compound facilitates the introduction of the 4-fluoropiperidine moiety into complex molecular structures, thereby imparting specific properties or functions.In chemical synthesis, 1-Boc-4-fluoropiperidine-4-carboxylic acid is commonly employed as a precursor for the synthesis of bioactive molecules and pharmaceutical intermediates. Its stability and reactivity make it an ideal starting material for the modification and functionalization of organic molecules, enabling chemists to create new compounds with tailored properties.Furthermore, the presence of the Boc protecting group offers added control over the reaction selectivity and allows for sequential transformations in multi-step synthesis processes. This compound's application extends to the synthesis of diverse heterocyclic compounds and natural product derivatives, making it indispensable in modern organic chemistry research and development.Overall, the strategic incorporation of 1-Boc-4-fluoropiperidine-4-carboxylic acid in chemical synthesis provides chemists with a powerful tool for accessing structurally diverse and biologically relevant compounds, driving innovation and advancements in the field of medicinal chemistry and beyond.