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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-ethoxypiperidine-1-carboxylate

CCOC1CCN(CC1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-ethoxypiperidine-1-carboxylate
CAS Number: 460367-82-2
Product Number: AG00DJLH(AGN-PC-09ZUSI)
Synonyms:
MDL No:
Molecular Formula: C12H23NO3
Molecular Weight: 229.3159

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
229.32g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
229.168g/mol
Monoisotopic Mass:
229.168g/mol
Topological Polar Surface Area:
38.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
227
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


tert-Butyl 4-ethoxypiperidine-1-carboxylate is a versatile compound widely used in chemical synthesis, particularly in the development of pharmaceuticals and specialty chemicals. This compound serves as a key building block in the creation of various bioactive molecules due to its unique structural properties and reactivity. In the realm of organic synthesis, tert-Butyl 4-ethoxypiperidine-1-carboxylate plays a crucial role as a protecting group that can mask reactive functional groups during complex synthetic procedures. This protection allows chemists to carry out selective reactions without unwanted side reactions or interferences, ultimately leading to higher yields and purities in the final products. Additionally, tert-Butyl 4-ethoxypiperidine-1-carboxylate can also function as a precursor in the synthesis of nitrogen-containing heterocycles, which are commonly found in many bioactive molecules. Its strategic incorporation in synthetic routes enables the efficient construction of diverse chemical structures with desired pharmacological activities.