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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)-

Formamide, N-octadecyl-

CCCCCCCCCCCCCCCCCCNC=O Request for Quotation
Chemical Name: Formamide, N-octadecyl-
CAS Number: 32585-06-1
Product Number: AG00CMT2(AGN-PC-0JP3GQ)
Synonyms:
MDL No:
Molecular Formula: C19H39NO
Molecular Weight: 297.51906

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Chemical Structure


N-Octadecylformamide is a versatile compound widely employed in chemical synthesis as a key intermediate in various reactions. Its aliphatic chain structure and formamide functional group make it an ideal starting material for the synthesis of diverse organic compounds. In particular, N-Octadecylformamide is frequently utilized as a precursor for the preparation of surfactants, emulsifiers, and lubricants due to its amphiphilic nature. Additionally, its ability to undergo amidation, esterification, and other functional group transformations further expands its utility in the production of specialty chemicals and pharmaceutical ingredients. Furthermore, N-Octadecylformamide serves as a valuable building block for the synthesis of advanced materials used in industries such as coatings, polymers, and agrochemicals. Its broad applicability and compatibility in various synthetic methodologies underscore its significance in the realm of chemical synthesis.