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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-(methoxymethyl)-

COCc1ncc[nH]1 Request for Quotation
Chemical Name: 1H-Imidazole, 2-(methoxymethyl)-
CAS Number: 102644-75-7
Product Number: AG00080M(AGN-PC-003HGE)
Synonyms:
MDL No:
Molecular Formula: C5H8N2O
Molecular Weight: 112.1298

Identification/Properties

Computed Properties
Molecular Weight:
112.132g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
112.064g/mol
Monoisotopic Mass:
112.064g/mol
Topological Polar Surface Area:
37.9A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
67.4
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


2-Methoxymethyl-1H-imidazole is a versatile chemical compound widely used in chemical synthesis. This compound serves as a valuable building block in organic chemistry due to its unique reactivity and functional groups. In particular, it is commonly employed as a reagent in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.One key application of 2-Methoxymethyl-1H-imidazole is its use in the formation of heterocyclic compounds. By undergoing various reactions such as nucleophilic substitutions, condensations, and cyclizations, this compound can be utilized to construct complex molecular frameworks containing nitrogen atoms. These nitrogen-containing heterocycles are crucial components in the design and development of biologically active molecules and materials.Furthermore, 2-Methoxymethyl-1H-imidazole can also participate in the synthesis of functionalized organic molecules. Its methoxymethyl group can serve as a protecting group for sensitive functional moieties, allowing selective manipulation of specific sites within a molecule. This feature enables chemists to control the progression of chemical reactions and enhance the efficiency of synthetic pathways.Overall, the versatile nature of 2-Methoxymethyl-1H-imidazole makes it a valuable tool in chemical synthesis, offering chemists the flexibility to create diverse compounds with tailored properties and functionalities.