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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 4-hydroxy-3-methylpiperidine-1-carboxylate

OC1CCN(CC1C)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-hydroxy-3-methylpiperidine-1-carboxylate
CAS Number: 181269-70-5
Product Number: AG0022RI(AGN-PC-093R09)
Synonyms:
MDL No:
Molecular Formula: C11H21NO3
Molecular Weight: 215.2893

Identification/Properties

Properties
BP:
301.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
215.293g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
215.152g/mol
Monoisotopic Mass:
215.152g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
235
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Boc-4-hydroxy-3-methylpiperidine is a versatile chemical compound commonly used in chemical synthesis for its unique properties. This compound serves as a valuable building block in organic synthesis, particularly in the field of pharmaceuticals and drug development.Due to its Boc (tert-butyloxycarbonyl) protecting group, 1-Boc-4-hydroxy-3-methylpiperidine is highly selective in reactions, allowing for precise control over functional group transformations. The Boc group can be easily removed under mild conditions, making it a valuable tool for the synthesis of complex molecules.In pharmaceutical research, this compound is frequently utilized in the synthesis of various biologically active compounds, such as inhibitors, ligands, and intermediates for drug candidates. Its structural features make it ideal for introducing specific functional groups or moieties into target molecules.Additionally, 1-Boc-4-hydroxy-3-methylpiperidine can participate in key carbon-carbon and carbon-nitrogen bond-forming reactions, enabling chemists to construct intricate molecular frameworks efficiently. Its compatibility with a wide range of reagents and reaction conditions enhances its usefulness in diverse synthetic pathways.Overall, the application of 1-Boc-4-hydroxy-3-methylpiperidine in chemical synthesis offers chemists a reliable and versatile tool for the construction of complex organic molecules with high precision and efficiency.