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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-carboxylic acid, 1-methyl-, hydrazide

NNC(=O)c1nccn1C Request for Quotation
Chemical Name: 1H-Imidazole-2-carboxylic acid, 1-methyl-, hydrazide
CAS Number: 33543-79-2
Product Number: AG007EYA(AGN-PC-01G49O)
Synonyms:
MDL No:
Molecular Formula: C5H8N4O
Molecular Weight: 140.1432

Identification/Properties

Computed Properties
Molecular Weight:
140.146g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
140.07g/mol
Monoisotopic Mass:
140.07g/mol
Topological Polar Surface Area:
72.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
138
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


1-Methyl-1H-imidazole-2-carbohydrazide, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis for a variety of applications. This compound serves as a key building block in the development of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique reactivity and structure.In chemical synthesis, 1-Methyl-1H-imidazole-2-carbohydrazide is utilized as a precursor in the formation of heterocyclic compounds, which are essential in drug discovery and development. Its ability to undergo various chemical transformations, such as acylation, alkylation, and cyclization reactions, makes it a valuable tool in the creation of complex organic molecules with specific biological activities.Furthermore, this compound plays a crucial role in the synthesis of peptide mimetics, which are designed to mimic the structure and function of peptides for therapeutic purposes. By incorporating 1-Methyl-1H-imidazole-2-carbohydrazide into the synthesis of peptide mimetics, chemists can tailor the properties of these molecules to enhance their stability, bioavailability, and target specificity.Overall, the application of 1-Methyl-1H-imidazole-2-carbohydrazide in chemical synthesis enables researchers to explore new avenues in drug design, material science, and other fields that require the creation of novel compounds with tailored properties and functions.