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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)-

5-AMINO-1-METHYL-3-PHENYLPYRAZOLE

Cn1nc(cc1N)c1ccccc1 Request for Quotation
Chemical Name: 5-AMINO-1-METHYL-3-PHENYLPYRAZOLE
CAS Number: 10199-50-5
Product Number: AG000665(AGN-PC-0WB2T2)
Synonyms:
MDL No:
Molecular Formula: C10H11N3
Molecular Weight: 173.2144

Identification/Properties

Properties
MP:
128 - 130°C
BP:
368.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
173.219g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
173.095g/mol
Monoisotopic Mass:
173.095g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
166
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-3-phenyl-1H-pyrazol-5-amine is a versatile compound widely utilized in chemical synthesis as a key building block for the creation of various organic molecules. In synthetic chemistry, this compound serves as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structural properties make it a vital component in the development of diverse chemical entities with specific functionalities and applications. Due to its reactivity and compatibility with different reaction conditions, 1-Methyl-3-phenyl-1H-pyrazol-5-amine plays a crucial role in the construction of complex molecular structures through multi-step synthesis strategies. Chemists leverage the distinct reactivity of this compound to introduce specific functional groups, facilitate molecular transformations, and enhance the efficiency of synthetic routes in various research and industrial settings.