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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)-

tert-butyl (3R,4S)-4-amino-3-fluoropiperidine-1-carboxylate

NC1CCN(CC1F)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl (3R,4S)-4-amino-3-fluoropiperidine-1-carboxylate
CAS Number: 934536-10-4
Product Number: AG00H0ZH(AGN-PC-005KH2)
Synonyms:
MDL No:
Molecular Formula: C10H19FN2O2
Molecular Weight: 218.2685

Identification/Properties

Computed Properties
Molecular Weight:
218.272g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
218.143g/mol
Monoisotopic Mass:
218.143g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
240
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


Tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate is a versatile compound widely utilized in chemical synthesis as a key building block for the creation of various compounds with pharmaceutical and agrochemical applications. Its unique structure and properties make it an essential component in the development of advanced chemical entities.One of the primary applications of tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate is in the synthesis of novel drug candidates. Due to its specific functional groups and stereochemistry, this compound serves as a crucial intermediate in the construction of biologically active molecules targeting various disease pathways. Its incorporation into synthetic routes enables the efficient production of diverse drug analogs with potential therapeutic benefits.Furthermore, tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate plays a significant role in the design and synthesis of agrochemicals. By utilizing this compound as a precursor, chemists can access a wide range of structurally diverse compounds that exhibit pesticidal, herbicidal, or fungicidal properties. The incorporation of this building block in agrochemical research programs enables the development of innovative solutions for crop protection and pest management.In conclusion, the application of tert-Butyl 4-amino-3-fluoropiperidine-1-carboxylate in chemical synthesis is instrumental in accelerating the discovery and development of new pharmaceuticals and agrochemicals. Its strategic use as a key intermediate empowers chemists to access complex molecular frameworks and advance the forefront of scientific innovation in the fields of medicine and agriculture.