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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-(3,5-dimethyl-1H-pyrazol-4-yl)-N-methylmethanamine

CNCc1c(C)n[nH]c1C Request for Quotation
Chemical Name: 1-(3,5-dimethyl-1H-pyrazol-4-yl)-N-methylmethanamine
CAS Number: 919347-92-5
Product Number: AG00GTT1(AGN-PC-05C9XJ)
Synonyms:
MDL No:
Molecular Formula: C7H13N3
Molecular Weight: 139.1982

Identification/Properties

Computed Properties
Molecular Weight:
139.202g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
139.111g/mol
Monoisotopic Mass:
139.111g/mol
Topological Polar Surface Area:
40.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
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


The compound 1-(3,5-Dimethyl-1H-pyrazol-4-yl)-N-methylmethanamine plays a crucial role in chemical synthesis as a versatile building block. Its unique structure allows for a variety of synthetic pathways, making it a valuable tool in the creation of complex organic molecules. This compound can be utilized in the development of novel pharmaceuticals, agrochemicals, and materials due to its ability to introduce specific functional groups with precision. Its presence in chemical reactions enables the formation of new carbon-carbon or carbon-nitrogen bonds, facilitating the construction of diverse molecular architectures. Additionally, its compatibility with various reaction conditions further expands its utility in synthetic transformations, highlighting its significance as a valuable intermediate in chemical synthesis processes.