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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-(4-methoxyphenyl)-1H-pyrazol-3-yl]methanamine hydrochloride

COc1ccc(cc1)n1ccc(n1)CN.Cl Request for Quotation
Chemical Name: [1-(4-methoxyphenyl)-1H-pyrazol-3-yl]methanamine hydrochloride
CAS Number: 1193388-04-3
Product Number: AG019WLW(AG019WLW)
Synonyms:
MDL No:
Molecular Formula: C11H14ClN3O
Molecular Weight: 239.7014

Identification/Properties

Computed Properties
Molecular Weight:
239.703g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
239.083g/mol
Monoisotopic Mass:
239.083g/mol
Topological Polar Surface Area:
53.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
192
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The [1-(4-Methoxyphenyl)-1H-pyrazol-3-yl]methanamine Hydrochloride compound plays a pivotal role in chemical synthesis due to its versatile applications. This unique compound serves as a vital building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. It is commonly utilized as a key intermediate in the synthesis of complex molecules with diverse biological activities.In organic synthesis, [1-(4-Methoxyphenyl)-1H-pyrazol-3-yl]methanamine Hydrochloride is frequently employed in the formation of carbon-carbon and carbon-nitrogen bonds through a series of strategic transformations. Its presence facilitates the construction of structurally intricate frameworks, allowing chemists to access a wide range of novel compounds with tailored properties and functions.Furthermore, the reactivity of [1-(4-Methoxyphenyl)-1H-pyrazol-3-yl]methanamine Hydrochloride enables the introduction of functional groups at specific positions within a molecule, thus enabling fine-tuning of its physicochemical characteristics. This compound's ability to participate in various catalytic and stoichiometric reactions makes it a valuable tool for synthetic chemists seeking to streamline the production of target molecules in a sustainable and efficient manner.