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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-ethyl 3-methylpiperidine-1,3-dicarboxylate

CCOC(=O)C1(C)CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-O-tert-butyl 3-O-ethyl 3-methylpiperidine-1,3-dicarboxylate
CAS Number: 278789-43-8
Product Number: AG003Q0J(AGN-PC-02WAFD)
Synonyms:
MDL No: MFCD11559117
Molecular Formula: C14H25NO4
Molecular Weight: 271.3526

Identification/Properties

Properties
BP:
329.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
271.357g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
271.178g/mol
Monoisotopic Mass:
271.178g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
348
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


Ethyl 1-Boc-3-methylpiperidine-3-carboxylate is a versatile compound commonly used in various chemical synthesis reactions. This compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a valuable tool in organic synthesis. Ethyl 1-Boc-3-methylpiperidine-3-carboxylate is particularly utilized in the preparation of complex molecules due to its ability to undergo various functional group transformations and reactions. Its application extends to the creation of heterocyclic compounds, chiral compounds, and bioactive molecules. This compound plays a crucial role in the development of new materials and compounds with potential applications in a wide range of industries.