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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)-

1H-Pyrazol-3-amine, 5-(2-pyridinyl)-

Nc1[nH]nc(c1)c1ccccn1 Request for Quotation
Chemical Name: 1H-Pyrazol-3-amine, 5-(2-pyridinyl)-
CAS Number: 92352-29-9
Product Number: AG00GS39(AGN-PC-0LU5AV)
Synonyms:
MDL No:
Molecular Formula: C8H8N4
Molecular Weight: 160.1759

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
160.18g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
160.075g/mol
Monoisotopic Mass:
160.075g/mol
Topological Polar Surface Area:
67.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
150
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-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-(Pyridin-2-yl)-1H-pyrazol-5-amine plays a crucial role in chemical synthesis for several applications. Its unique structural properties make it a versatile building block in the creation of various organic compounds. In particular, this compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials. Due to its functional groups and reactivity, it can participate in a wide range of reactions such as cross-coupling, cycloaddition, and heterocycle formation. By incorporating 3-(Pyridin-2-yl)-1H-pyrazol-5-amine into synthetic routes, chemists can access a diverse array of complex molecules with potential biological or industrial significance.