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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-4-carboxylic acid, 5-methyl-

Cc1nc[nH]c1C(=O)O Request for Quotation
Chemical Name: 1H-Imidazole-4-carboxylic acid, 5-methyl-
CAS Number: 1457-59-6
Product Number: AG001DBV(AGN-PC-0JLB7T)
Synonyms:
MDL No:
Molecular Formula: C5H6N2O2
Molecular Weight: 126.1133

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
126.115g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
126.043g/mol
Monoisotopic Mass:
126.043g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
126
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


4-Methyl-1H-imidazole-5-carboxylic acid is a versatile compound that finds extensive application in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. Due to its unique structure and reactivity, this compound serves as a crucial building block for the synthesis of various pharmaceutical intermediates, leading to the development of new drugs and agrochemicals.One of the primary applications of 4-Methyl-1H-imidazole-5-carboxylic acid is in the synthesis of anti-inflammatory drugs. By incorporating this compound into the molecular structure of drug candidates, chemists can modulate the activity and selectivity of the resulting compounds, ultimately improving their therapeutic effects.Additionally, 4-Methyl-1H-imidazole-5-carboxylic acid plays a key role in the synthesis of herbicides and pesticides. Its functional groups enable the attachment of specific chemical moieties that enhance the herbicidal or pesticidal properties of the final products, making them more effective in controlling pests and weeds.Furthermore, this compound can be utilized in the preparation of fluorescent dyes and labeling agents for biological research applications. By incorporating 4-Methyl-1H-imidazole-5-carboxylic acid into the dye molecule, researchers can achieve desirable fluorescent properties that are crucial for various imaging and detection techniques in biological studies.Overall, the diverse applications of 4-Methyl-1H-imidazole-5-carboxylic acid in chemical synthesis highlight its significance in the pharmaceutical, agrochemical, and research fields, where its unique properties contribute to the development of novel compounds with valuable applications.