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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-pyridin-3-ylpiperidin-4-amine

NC1CCN(CC1)c1cccnc1 Request for Quotation
Chemical Name: 1-pyridin-3-ylpiperidin-4-amine
CAS Number: 933760-08-8
Product Number: AG003KND(AGN-PC-04PCV0)
Synonyms:
MDL No: MFCD09928096
Molecular Formula: C10H15N3
Molecular Weight: 177.2462

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
177.251g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
177.127g/mol
Monoisotopic Mass:
177.127g/mol
Topological Polar Surface Area:
42.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
152
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Amino-1-(3-pyridyl)piperidine, also known as 3-(Pyridin-3-yl)piperidin-4-amine, is a valuable chemical compound widely employed in the field of chemical synthesis. It serves as a versatile building block in organic chemistry due to its unique structure and reactivity.One of the key applications of 4-Amino-1-(3-pyridyl)piperidine is its role as a key intermediate in the synthesis of pharmaceutical compounds. This compound can be used as a precursor in the preparation of various bioactive molecules, including drugs and medicinal products. Its presence in the synthesis of heterocyclic compounds contributes to the development of novel pharmaceutical agents with diverse pharmacological activities.Furthermore, 4-Amino-1-(3-pyridyl)piperidine can be utilized in the construction of complex organic molecules through various chemical transformations. Its amino and pyridyl moieties provide sites for selective functionalization, enabling the introduction of different substituents or structural motifs. This flexibility makes it a valuable tool for organic chemists seeking to design and create molecular libraries with potential biological or material applications.In summary, 4-Amino-1-(3-pyridyl)piperidine plays a crucial role in chemical synthesis, particularly in the preparation of biologically active molecules and the design of structurally diverse compounds with potential therapeutic or industrial relevance. Its versatile reactivity and functionality make it a valuable building block for the creation of new materials and compounds in the field of organic chemistry.