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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)-

2-[(4-methoxyphenyl)methyl]-5-methylpyrazol-3-amine

COc1ccc(cc1)Cn1nc(cc1N)C Request for Quotation
Chemical Name: 2-[(4-methoxyphenyl)methyl]-5-methylpyrazol-3-amine
CAS Number: 949556-61-0
Product Number: AG006QS1(AGN-PC-0424PZ)
Synonyms:
MDL No:
Molecular Formula: C12H15N3O
Molecular Weight: 217.2670

Identification/Properties

Computed Properties
Molecular Weight:
217.272g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
217.122g/mol
Monoisotopic Mass:
217.122g/mol
Topological Polar Surface Area:
53.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
216
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Methoxybenzyl)-3-methyl-1H-pyrazol-5-amine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. In the field of organic chemistry, this compound serves as a key building block for the synthesis of various biologically active molecules and pharmaceutical intermediates. Its functional groups enable it to participate in a wide range of reactions, including nucleophilic substitution, condensation, and metal-catalyzed coupling reactions.Specifically, 1-(4-Methoxybenzyl)-3-methyl-1H-pyrazol-5-amine is often employed in the development of novel heterocyclic compounds. By utilizing its amino and methyl groups, chemists can introduce additional substituents to tailor the compound's properties for specific applications. Furthermore, its benzyl moiety provides a reactive handle for further functionalization, allowing for the attachment of various functional groups to modulate the compound's reactivity and selectivity.Overall, the diverse applications of 1-(4-Methoxybenzyl)-3-methyl-1H-pyrazol-5-amine in chemical synthesis make it an indispensable tool for the design and synthesis of complex organic molecules with potential therapeutic or industrial significance.