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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)-

1H-Pyrazole-1-ethanamine, 4-iodo-N,N-dimethyl-

CN(CCn1ncc(c1)I)C Request for Quotation
Chemical Name: 1H-Pyrazole-1-ethanamine, 4-iodo-N,N-dimethyl-
CAS Number: 879488-19-4
Product Number: AG004D56(AGN-PC-0FSC9Y)
Synonyms:
MDL No:
Molecular Formula: C7H12IN3
Molecular Weight: 265.0948

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
265.098g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
265.008g/mol
Monoisotopic Mass:
265.008g/mol
Topological Polar Surface Area:
21.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
118
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Iodo-1H-pyrazol-1-yl)-N,N-dimethylethanamine is a versatile compound that finds wide application in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block in the creation of various organic molecules. In particular, this compound is frequently utilized in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to undergo selective reactions and form stable intermediates makes it an essential component in the creation of complex organic compounds. Researchers and chemists often rely on 2-(4-Iodo-1H-pyrazol-1-yl)-N,N-dimethylethanamine to introduce specific functional groups or motifs into target molecules, enabling the production of novel compounds with enhanced properties and activities. Additionally, its compatibility with a wide range of reaction conditions and protocols further enhances its utility in chemical synthesis, making it a valuable tool for the development of new materials and substances.