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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-(1-methyl-1H-pyrazol-4-yl)propan-2-amine

Cn1ncc(c1)C(N)(C)C Request for Quotation
Chemical Name: 2-(1-methyl-1H-pyrazol-4-yl)propan-2-amine
CAS Number: 1215936-45-0
Product Number: AG01AKVS(AGN-PC-0WO0BB)
Synonyms:
MDL No: MFCD11899126
Molecular Formula: C7H13N3
Molecular Weight: 139.1982

Identification/Properties

Computed Properties
Molecular Weight:
139.202g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
139.111g/mol
Monoisotopic Mass:
139.111g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
122
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


2-(1-Methyl-1H-pyrazol-4-yl)propan-2-amine, also known as $name$, is a versatile compound that finds significant utility in chemical synthesis processes. As an amine derivative, this compound serves as a crucial building block for the creation of various organic molecules through its involvement in a multitude of synthetic reactions. $name$ is commonly employed in the formation of complex heterocyclic structures due to its pyrazole moiety, which imparts desirable properties and functionalities to the target molecules. Additionally, the presence of the propylamine group enhances the reactivity and selectivity of $name$ in a wide range of synthetic transformations.In chemical synthesis, $name$ can act as both a nucleophile and a ligand, facilitating reactions such as acylation, alkylation, and condensation. Its ability to participate in diverse chemical processes makes it a valuable tool for the preparation of pharmaceuticals, agrochemicals, and materials with tailored properties.Overall, the unique structure and reactivity of 2-(1-Methyl-1H-pyrazol-4-yl)propan-2-amine make it an indispensable component in the toolkit of synthetic chemists, enabling the efficient construction of novel and structurally complex molecules.