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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)-

2-Piperidinepropanoic acid, 1-[(1,1-dimethylethoxy)carbonyl]-

OC(=O)CCC1CCCCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2-Piperidinepropanoic acid, 1-[(1,1-dimethylethoxy)carbonyl]-
CAS Number: 669713-96-6
Product Number: AG006N4F(AGN-PC-0KKLBC)
Synonyms:
MDL No:
Molecular Formula: C13H23NO4
Molecular Weight: 257.3260

Identification/Properties

Properties
BP:
386.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
257.33g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
257.163g/mol
Monoisotopic Mass:
257.163g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
309
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


A versatile compound, $name$ plays a crucial role in chemical synthesis as a key building block for the production of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, containing a tert-butoxycarbonyl-protected piperidine moiety, affords exceptional reactivity and selectivity in multi-step synthetic pathways.Firstly, $name$ serves as a valuable intermediate in the synthesis of diverse pharmaceutical compounds due to its ability to participate in a variety of key reactions, such as amidation, esterification, and hydrogenation. Additionally, the presence of the tert-butoxycarbonyl protective group ensures that the piperidine ring remains intact during subsequent transformations, enabling precise control over regioselectivity and stereoselectivity.Furthermore, $name$ finds application in the development of agrochemicals by enabling the construction of complex structural motifs found in pesticides, herbicides, and fungicides. Its compatibility with various functional groups allows for the incorporation of specific characteristics necessary for the desired biological activity of the end products.In the field of materials science, $name$ is utilized in the synthesis of advanced materials with tailored properties, such as polymers, surfactants, and catalysts. The presence of the piperidine moiety enhances the compatibility of the compound with various polymerization techniques, enabling the production of high-performance materials with controlled molecular weight and architecture.Overall, the versatile nature of $name$ makes it an indispensable tool in chemical synthesis, facilitating the construction of complex molecular structures with precision and efficiency. Its wide-ranging applications across pharmaceuticals, agrochemicals, and materials science highlight its importance in advancing research and innovation in the field of chemistry.