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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)-

(6-pyrazol-1-ylpyridin-3-yl)methanamine

NCc1ccc(nc1)n1cccn1 Request for Quotation
Chemical Name: (6-pyrazol-1-ylpyridin-3-yl)methanamine
CAS Number: 956191-88-1
Product Number: AG00IJ8Y(AGN-PC-00UXIN)
Synonyms:
MDL No: MFCD08691193
Molecular Formula: C9H10N4
Molecular Weight: 174.2025

Identification/Properties

Computed Properties
Molecular Weight:
174.207g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
174.091g/mol
Monoisotopic Mass:
174.091g/mol
Topological Polar Surface Area:
56.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
162
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:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Aminomethyl)-2-(1-pyrazolyl)pyridine plays a crucial role in chemical synthesis due to its versatile reactivity and unique structural properties. This compound serves as a valuable building block in the creation of various organic compounds, particularly in medicinal chemistry and materials science. Its amino and pyridine functionalities make it a key intermediate in the development of pharmaceuticals, agrochemicals, and complex organic molecules. Furthermore, the presence of the pyrazole ring enhances the compound's biological activity and potential for the synthesis of novel drug candidates. In the field of chemical synthesis, 5-(Aminomethyl)-2-(1-pyrazolyl)pyridine serves as a versatile starting material for the creation of diverse molecular scaffolds and functional groups, enabling the design and production of advanced materials with enhanced properties and applications.