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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)-

Pyridine, 2-methyl-6-(1H-pyrazol-3-yl)-

Cc1cccc(n1)c1n[nH]cc1 Request for Quotation
Chemical Name: Pyridine, 2-methyl-6-(1H-pyrazol-3-yl)-
CAS Number: 203569-23-7
Product Number: AG0028ZF(AGN-PC-0O7B6X)
Synonyms:
MDL No:
Molecular Formula: C9H9N3
Molecular Weight: 159.1879

Identification/Properties

Computed Properties
Molecular Weight:
159.192g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
159.08g/mol
Monoisotopic Mass:
159.08g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
149
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-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyl-6-(1H-pyrazol-3-yl)pyridine, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block for various organic compounds. With its unique structure combining a pyridine and pyrazole ring, this compound exhibits diverse reactivity that enables its use in the creation of pharmaceuticals, agrochemicals, and materials. In chemical synthesis, $name$ serves as a key intermediate in the preparation of complex molecules by participating in selective cross-coupling reactions, cyclization processes, and metal-catalyzed transformations. Its ability to undergo functional group modifications makes it a valuable tool for the construction of novel compounds with desired properties. In addition, the presence of the pyrazole moiety in $name$ imparts bioactivity to the synthesized molecules, making it a significant component in the development of potentially therapeutic agents and other biologically active substances.