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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)-

Octane, 1-(chloromethoxy)-

CCCCCCCCOCCl Request for Quotation
Chemical Name: Octane, 1-(chloromethoxy)-
CAS Number: 24566-90-3
Product Number: AG002OL7(AGN-PC-0JSHYB)
Synonyms:
MDL No:
Molecular Formula: C9H19ClO
Molecular Weight: 178.6996

Identification/Properties

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NMR Spectrum

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Chemical Structure


$name$ is a versatile chemical compound primarily used in chemical synthesis as an important building block. One of its key applications is in organic chemistry reactions, where it serves as an efficient alkylating agent. Chloromethyloctylether can be utilized in various reactions to introduce the octyl group into organic molecules, thereby modifying their structure and properties. Specifically, it is commonly employed in the synthesis of complex organic compounds, where the octyl group is strategically incorporated for specific functionality or reactivity. Its reactivity and selectivity in alkylating reactions make it a valuable tool for chemists working on the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the unique structure of Chloromethyloctylether makes it suitable for use in the development of new molecules with tailored properties, expanding the possibilities for chemical synthesis and innovation.