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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-(1,3,5-trimethylpyrazol-4-yl)ethanamine

CC(c1c(C)nn(c1C)C)N Request for Quotation
Chemical Name: 1-(1,3,5-trimethylpyrazol-4-yl)ethanamine
CAS Number: 936940-12-4
Product Number: AG00GVTP(AGN-PC-02GBGU)
Synonyms:
MDL No:
Molecular Formula: C8H15N3
Molecular Weight: 153.2248

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
153.229g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
153.127g/mol
Monoisotopic Mass:
153.127g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
137
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1-(1,3,5-Trimethyl-1H-pyrazol-4-yl)ethanamine is a versatile compound widely employed in chemical synthesis as a building block for the preparation of various functional molecules. Its primary application lies in organic chemistry, where it serves as a key intermediate for the synthesis of diverse organic compounds. The unique structure of this compound enables it to participate in a range of reactions, making it valuable for the creation of complex chemical structures. In particular, 1-(1,3,5-Trimethyl-1H-pyrazol-4-yl)ethanamine is utilized in the development of pharmaceuticals, agrochemicals, and materials science due to its ability to introduce specific functionalities into target molecules. Additionally, its reactivity and compatibility with a variety of other reagents make it a valuable tool in the hands of synthetic chemists seeking to design and construct novel molecules with tailored properties.