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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)-

Acetyl chloride, (2,6-dimethylphenoxy)-

ClC(=O)COc1c(C)cccc1C Request for Quotation
Chemical Name: Acetyl chloride, (2,6-dimethylphenoxy)-
CAS Number: 20143-48-0
Product Number: AG00C29A(AGN-PC-0NIPTN)
Synonyms:
MDL No:
Molecular Formula: C10H11ClO2
Molecular Weight: 198.64614

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Chemical Structure


(2,6-Dimethylphenoxy)acetyl chloride is a versatile compound used in chemical synthesis for various applications. In organic chemistry, it serves as a key reagent in the acylation of various nucleophiles, such as alcohols, amines, and thiols, to introduce the (2,6-dimethylphenoxy)acetyl group. This acetylating agent can be utilized in the preparation of complex organic molecules, pharmaceutical intermediates, and agrochemicals through acylation reactions. Its high reactivity and selectivity make it a valuable tool for modifying and functionalizing organic compounds in synthetic pathways. Additionally, (2,6-Dimethylphenoxy)acetyl chloride is employed in the production of specialty chemicals, fine chemicals, and materials for research and industrial applications.