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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-Piperidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester

OC1CCCN(C1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 3-hydroxy-, phenylmethyl ester
CAS Number: 95798-22-4
Product Number: AG006AXX(AGN-PC-0JSX52)
Synonyms:
MDL No: MFCD03839903
Molecular Formula: C13H17NO3
Molecular Weight: 235.2790

Identification/Properties

Properties
BP:
384.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
235.283g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
235.121g/mol
Monoisotopic Mass:
235.121g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
251
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzyl 3-hydroxypiperidine-1-carboxylate is a versatile compound that plays a crucial role in chemical synthesis. This compound is commonly utilized as a key building block in the preparation of various pharmaceuticals and fine chemicals. Due to its unique structure, Benzyl 3-hydroxypiperidine-1-carboxylate serves as an important intermediate in the synthesis of biologically active molecules.One of the prominent applications of Benzyl 3-hydroxypiperidine-1-carboxylate is in the manufacturing of pharmaceuticals, particularly those targeting the central nervous system. This compound can be used to introduce specific functional groups or modify existing structures, thereby enhancing the biological activity or improving the pharmacokinetic properties of the final drug product. Additionally, Benzyl 3-hydroxypiperidine-1-carboxylate can be employed in the synthesis of specialized chemicals for research purposes, contributing to advancements in medicinal chemistry and drug discovery.In chemical synthesis, Benzyl 3-hydroxypiperidine-1-carboxylate serves as a valuable tool for organic chemists seeking to access diverse molecular scaffolds and explore new chemical reactions. Its reactivity and compatibility with various synthetic methods make it a versatile starting material for the construction of complex molecules with specific functionalities. By incorporating Benzyl 3-hydroxypiperidine-1-carboxylate into synthetic pathways, chemists can efficiently access structurally diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.