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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-Piperidinecarboxylic acid, 3-amino-, 1,1-dimethylethyl ester

NC1CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 3-amino-, 1,1-dimethylethyl ester
CAS Number: 184637-48-7
Product Number: AG00I1IE(AGN-PC-0JSNZV)
Synonyms:
MDL No: MFCD01861219
Molecular Formula: C10H20N2O2
Molecular Weight: 200.278

Identification/Properties

Properties
MP:
181-182°C
BP:
277.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Stability:
Air Sensitive
Refractive Index:
1.4710-1.4750
Computed Properties
Molecular Weight:
200.282g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
200.152g/mol
Monoisotopic Mass:
200.152g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
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+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Amino-1-N-Boc-Piperidine is a versatile compound widely used in chemical synthesis for various applications. This compound serves as a key building block in the pharmaceutical industry for the synthesis of a variety of bioactive molecules and drug candidates. Due to its unique structure and reactivity, 3-Amino-1-N-Boc-Piperidine plays a crucial role in the development of pharmaceuticals and agrochemicals. In organic synthesis, it can be utilized as a nucleophilic amine for the preparation of functionalized piperidine derivatives. Additionally, 3-Amino-1-N-Boc-Piperidine can be employed in the production of complex heterocyclic compounds through multiple synthetic pathways, making it a valuable tool in medicinal chemistry and drug discovery efforts.