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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, 4-hydroxy-, phenylmethyl ester

OC1CCN(CC1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 4-hydroxy-, phenylmethyl ester
CAS Number: 95798-23-5
Product Number: AG003O3Q(AGN-PC-0KL6ZI)
Synonyms:
MDL No: MFCD01863722
Molecular Formula: C13H17NO3
Molecular Weight: 235.2790

Identification/Properties

Properties
BP:
384.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
n20/D 1.543(lit.)
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:
243
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:
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


Benzyl 4-hydroxypiperidine-1-carboxylate is a versatile compound commonly used in chemical synthesis as a key intermediate. Its unique structure and reactivity make it particularly valuable in the field of organic chemistry. One of the main applications of Benzyl 4-hydroxypiperidine-1-carboxylate is in the synthesis of various pharmaceutical compounds. Its functional groups can undergo a range of chemical reactions, allowing for the formation of diverse molecular structures. This flexibility makes it a valuable building block for the creation of new drug candidates and bioactive molecules.Furthermore, Benzyl 4-hydroxypiperidine-1-carboxylate can also be utilized in the development of agrochemicals and specialty chemicals. Its ability to undergo selective transformations enables the production of complex and structurally diverse compounds with specific properties.Overall, Benzyl 4-hydroxypiperidine-1-carboxylate serves as a crucial tool in the hands of synthetic chemists, offering a high degree of control and versatility in the design and construction of novel chemical entities. Its role in chemical synthesis extends beyond the pharmaceutical industry, finding applications in various sectors where tailored molecules are required for specific purposes.