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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)-

Thiazolium, 5-(2-hydroxyethyl)-3,4-dimethyl-, iodide

Cc1c(CCO)sc[n+]1C.[I-] Request for Quotation
Chemical Name: Thiazolium, 5-(2-hydroxyethyl)-3,4-dimethyl-, iodide
CAS Number: 16311-69-6
Product Number: AG001TSD(AGN-PC-0MUCWP)
Synonyms:
MDL No:
Molecular Formula: C7H12INOS
Molecular Weight: 285.1458

Identification/Properties

Computed Properties
Molecular Weight:
285.143g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
284.968g/mol
Monoisotopic Mass:
284.968g/mol
Topological Polar Surface Area:
52.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
110
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound $name$ (3,4-Dimethyl-5-(2-hydroxyethyl)thiazolium iodide) is a versatile reagent widely utilized in chemical synthesis processes. Its application in organic chemistry allows for the efficient introduction of functional groups and modification of target molecules. One key use of this compound is as a versatile organocatalyst in various reactions, including Mannich-type reactions, aldol condensations, and Knoevenagel condensations. Additionally, $name$ is often employed in the synthesis of pharmaceutical intermediates, natural products, and fine chemicals due to its unique reactivity and selectivity in catalyzing complex transformations. Its ability to facilitate the formation of C-C and C-N bonds makes it a valuable tool in the organic synthesis toolbox.