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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-methyl-4-oxopiperidine-1,3-dicarboxylate

COC(=O)C1(C)CN(CCC1=O)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-O-tert-butyl 3-O-methyl 3-methyl-4-oxopiperidine-1,3-dicarboxylate
CAS Number: 193274-53-2
Product Number: AG00AQO6(AGN-PC-0H9BQM)
Synonyms:
MDL No:
Molecular Formula: C13H21NO5
Molecular Weight: 271.3095

Identification/Properties

Properties
MP:
42-43℃
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
271.313g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
271.142g/mol
Monoisotopic Mass:
271.142g/mol
Topological Polar Surface Area:
72.9A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
398
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 1-Boc-3-methyl-4-oxo-piperidine-3-carboxylate, often referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its incorporation in various chemical reactions allows for the synthesis of complex molecules with specific structural features. This compound is commonly utilized as a protective group for amines due to the stability of the Boc (tert-butoxycarbonyl) group. In addition, the presence of the methyl and ester functional groups enables $name$ to participate in a range of chemical transformations, making it highly valuable in organic synthesis.