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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-Imidazole, 2,4-dimethyl-

Cc1[nH]cc(n1)C Request for Quotation
Chemical Name: 1H-Imidazole, 2,4-dimethyl-
CAS Number: 930-62-1
Product Number: AG0032ZR(AGN-PC-0ONJA1)
Synonyms:
MDL No:
Molecular Formula: C5H8N2
Molecular Weight: 96.1304

Identification/Properties

Properties
MP:
85-87 °C
BP:
267.0°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5000 (estimate)
Computed Properties
Molecular Weight:
96.133g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
96.069g/mol
Monoisotopic Mass:
96.069g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
63.1
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:
Danger
UN#:
3263
Hazard Statements:
H302-H314
Precautionary Statements:
P261-P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dimethylimidazole is widely used in chemical synthesis as a versatile building block due to its unique properties. It serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its chemical structure allows for facile modification and functionalization, making it highly valuable in organic synthesis.This compound is specifically utilized as a catalyst or ligand in a range of organic reactions, including asymmetric catalysis, metal-catalyzed coupling reactions, and organometallic transformations. Its chelating abilities and versatile reactivity enable it to participate in a diverse array of reactions, leading to the synthesis of complex molecules with high efficiency and selectivity.In addition, 2,4-Dimethylimidazole plays a crucial role in the development of novel materials such as polymers, dyes, and coordination complexes. Its ability to coordinate with metal ions and form stable complexes is exploited in the design of functional materials with tailored properties for various industrial applications.Overall, the application of 2,4-Dimethylimidazole in chemical synthesis is fundamental to the advancement of modern organic chemistry, enabling the streamlined and efficient construction of intricate molecular structures and functional materials.