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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)-

methyl 4-hydroxypiperidine-3-carboxylate

COC(=O)C1CNCCC1O Request for Quotation
Chemical Name: methyl 4-hydroxypiperidine-3-carboxylate
CAS Number: 959958-24-8
Product Number: AG00IJPO(AGN-PC-00L0L4)
Synonyms:
MDL No: MFCD09910302
Molecular Formula: C7H13NO3
Molecular Weight: 159.1830

Identification/Properties

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


Methyl 4-hydroxypiperidine-3-carboxylate is a versatile compound widely utilized in chemical synthesis, particularly in the pharmaceutical and fine chemicals industries. Its unique structure containing a piperidine ring and a carboxylic ester group lends itself to a variety of synthetic applications.One key application of Methyl 4-hydroxypiperidine-3-carboxylate is as a building block in the synthesis of pharmaceutical compounds. By providing a reactive site for further functionalization, this compound serves as a valuable intermediate in the production of various drugs and biologically active molecules. Its presence in the molecular structure can impart desirable pharmacological properties or improve the overall efficacy of the final product.Additionally, Methyl 4-hydroxypiperidine-3-carboxylate can be used in the preparation of complex organic molecules through multistep synthesis routes. Its compatibility with a range of synthetic methodologies enables chemists to access diverse chemical scaffolds, making it a valuable tool for creating novel compounds with potential applications in drug discovery, materials science, and agrochemicals.Furthermore, this compound's stability under typical reaction conditions and its ease of purification make it a preferred choice for chemical synthesis. Whether utilized in traditional organic transformations or modern synthetic strategies, Methyl 4-hydroxypiperidine-3-carboxylate plays a crucial role in advancing the field of chemistry and accelerating the development of innovative molecules with important industrial and academic significance.