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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-O-tert-butyl 3-O-methyl 3-methylpiperidine-1,3-dicarboxylate

COC(=O)C1(C)CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-O-tert-butyl 3-O-methyl 3-methylpiperidine-1,3-dicarboxylate
CAS Number: 888952-55-4
Product Number: AG003RK1(AGN-PC-080U0Z)
Synonyms:
MDL No: MFCD11977502
Molecular Formula: C13H23NO4
Molecular Weight: 257.3260

Identification/Properties

Properties
BP:
313.208°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
257.33g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
257.163g/mol
Monoisotopic Mass:
257.163g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
334
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 1-Boc-3-methylpiperidine-3-carboxylate is a versatile compound commonly employed in chemical synthesis as a key building block. This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential component for the construction of complex organic molecules in the laboratory.One of the main applications of Methyl 1-Boc-3-methylpiperidine-3-carboxylate is in the preparation of heterocyclic compounds, which are widely used in the pharmaceutical industry. By utilizing this compound as a starting material, chemists can access a diverse range of heterocycles through strategic synthetic transformations. These heterocyclic compounds often exhibit valuable biological activities, making them important targets for drug discovery and development.In addition to heterocyclic synthesis, Methyl 1-Boc-3-methylpiperidine-3-carboxylate can also be utilized in the construction of chiral molecules. Its chiral center provides a handle for stereochemical control, enabling the synthesis of enantiomerically pure compounds. This is particularly important in medicinal chemistry, where the biological activity of a molecule is often dependent on its stereochemistry.Overall, Methyl 1-Boc-3-methylpiperidine-3-carboxylate plays a crucial role in modern chemical synthesis, facilitating the efficient and selective construction of complex organic molecules with diverse applications.