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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)-

ethyl (3R)-1-aminopiperidine-3-carboxylate

CCOC(=O)C1CCCN(C1)N Request for Quotation
Chemical Name: ethyl (3R)-1-aminopiperidine-3-carboxylate
CAS Number: 938458-88-9
Product Number: AG00GVL1(AGN-PC-05RVHM)
Synonyms:
MDL No:
Molecular Formula: C8H16N2O2
Molecular Weight: 172.2248

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
172.228g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
172.121g/mol
Monoisotopic Mass:
172.121g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
161
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 1-aminopiperidine-3-carboxylate is a versatile compound that finds widespread application in chemical synthesis. This compound can be utilized as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and functional groups make it a valuable intermediate in the production of complex organic molecules.One of the primary uses of ethyl 1-aminopiperidine-3-carboxylate is in the synthesis of pharmaceutical compounds. By incorporating this compound into a synthesis route, chemists can access a range of bioactive molecules with potential therapeutic properties. The presence of the aminopiperidine moiety in the structure imparts specific biological activities to the final products, making it a crucial component in drug discovery and development.Furthermore, ethyl 1-aminopiperidine-3-carboxylate can serve as a precursor in the preparation of advanced materials and specialty chemicals. Its reactivity and compatibility with various functional groups allow for the construction of diverse molecular architectures. This compound can participate in a variety of chemical transformations, including acylation, alkylation, and cyclization reactions, enabling chemists to access structurally complex compounds efficiently.Overall, the versatility and synthetic utility of ethyl 1-aminopiperidine-3-carboxylate make it an indispensable tool in the realm of chemical synthesis. Its ability to serve as a linchpin in the construction of complex molecules underscores its significance in the development of new materials, pharmaceuticals, and other valuable products.