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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)-

(4-bromo-1-methylpyrazol-3-yl)methanamine

NCc1nn(cc1Br)C Request for Quotation
Chemical Name: (4-bromo-1-methylpyrazol-3-yl)methanamine
CAS Number: 926921-71-3
Product Number: AG006ERF(AGN-PC-02H38K)
Synonyms:
MDL No:
Molecular Formula: C5H8BrN3
Molecular Weight: 190.0411

Identification/Properties

Computed Properties
Molecular Weight:
190.044g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
188.99g/mol
Monoisotopic Mass:
188.99g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
98.2
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Application of (4-Bromo-1-methyl-1H-pyrazol-3-yl)methanamine in Chemical Synthesis:- Introduction into a multitude of chemical transformations, (4-Bromo-1-methyl-1H-pyrazol-3-yl)methanamine serves as a versatile building block in chemical synthesis. 
- it can be readily utilized in the creation of various heterocyclic compounds, which are pivotal in the development of pharmaceuticals, agrochemicals, and materials science.
- Its presence in the molecule allows for the introduction of diverse functional groups, enhancing the structural complexity and diversity of the final products. 
- The (4-Bromo-1-methyl-1H-pyrazol-3-yl)methanamine moiety is instrumental in facilitating key bond formations, enabling the synthesis of novel compounds with desired properties. 
- In medicinal chemistry, this compound can be employed in the synthesis of potential drug candidates or pharmacophores, thereby contributing to the exploration of new therapeutic agents.