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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)-

3-methylimidazole-4-carbonyl chloride;hydrochloride

Cn1cncc1C(=O)Cl.Cl Request for Quotation
Chemical Name: 3-methylimidazole-4-carbonyl chloride;hydrochloride
CAS Number: 343569-06-2
Product Number: AG00BZ22(AGN-PC-0KKXM3)
Synonyms:
MDL No:
Molecular Formula: C5H6Cl2N2O
Molecular Weight: 181.0199

Identification/Properties

Properties
MP:
214 °C
Form:
Solid
Computed Properties
Molecular Weight:
181.016g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
179.986g/mol
Monoisotopic Mass:
179.986g/mol
Topological Polar Surface Area:
34.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
128
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3261
Hazard Statements:
H314-H318
Precautionary Statements:
P280-P301+P330+P331-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-1H-imidazole-5-carbonyl chloride hydrochloride, commonly known as $name$, is a versatile compound widely used in chemical synthesis. It serves as an important building block in the development of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique reactivity and functional groups. In organic synthesis, $name$ is often employed as a key intermediate in the preparation of various complex molecules, including heterocyclic compounds, peptides, and natural products. Its ability to undergo selective reactions, such as acylation and nucleophilic substitution, makes it a valuable tool for skilled chemists seeking to tailor specific molecular structures. Additionally, the hydrochloride salt form of $name$ offers enhanced stability and solubility, facilitating its integration into diverse synthetic routes with improved efficiency and reproducibility.