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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-(3-methoxyphenyl)-

COc1cccc(c1)c1n[nH]c(c1)N Request for Quotation
Chemical Name: 1H-Pyrazol-3-amine, 5-(3-methoxyphenyl)-
CAS Number: 96799-04-1
Product Number: AG005STM(AGN-PC-0KZIBO)
Synonyms:
MDL No:
Molecular Formula: C10H11N3O
Molecular Weight: 189.2138

Identification/Properties

Properties
BP:
456.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
189.218g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
189.09g/mol
Monoisotopic Mass:
189.09g/mol
Topological Polar Surface Area:
63.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
188
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:
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


The compound 5-(3-Methoxyphenyl)-2H-pyrazol-3-ylamine, also known as $name$, is a versatile chemical reagent widely used in organic synthesis. Its unique structure and reactivity make it a valuable tool in the preparation of diverse molecules with applications in pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, $name$ serves as a key building block for the construction of complex molecules due to its ability to participate in a variety of important reactions. Its amino group can act as a nucleophile in substitution reactions, while the pyrazole ring provides a platform for further functionalization through various transformations. Additionally, the methoxyphenyl group can serve as a directing group in selective reactions, enabling precise control over regioselectivity and stereoselectivity.One of the primary applications of 5-(3-Methoxyphenyl)-2H-pyrazol-3-ylamine in chemical synthesis is in the preparation of heterocyclic compounds, which are prevalent in drug discovery and development. By incorporating $name$ into a synthetic pathway, chemists can access a wide range of bioactive molecules with diverse pharmacological properties. Furthermore, its structural features make it a valuable intermediate for the synthesis of natural products and functional materials with tailored properties.Overall, the versatility and reactivity of 5-(3-Methoxyphenyl)-2H-pyrazol-3-ylamine make it an indispensable tool for organic chemists seeking to access new molecular scaffolds and explore novel chemical space in the pursuit of scientific advancement and innovation.