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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)-

Dodecanamide, N-(2-hydroxyethyl)-

CCCCCCCCCCCC(=O)NCCO Request for Quotation
Chemical Name: Dodecanamide, N-(2-hydroxyethyl)-
CAS Number: 142-78-9
Product Number: AG0039O4(AGN-PC-0JK8RR)
Synonyms:
MDL No:
Molecular Formula: C14H29NO2
Molecular Weight: 243.3856

Identification/Properties

Computed Properties
Molecular Weight:
243.391g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
12
Exact Mass:
243.22g/mol
Monoisotopic Mass:
243.22g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
172
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(2-Hydroxyethyl)dodecanamide is a versatile compound commonly used in chemical synthesis processes. Its primary application lies in serving as a key intermediate in the production of various organic compounds. This compound is particularly valued for its ability to facilitate the synthesis of complex molecules with specific properties and functions.In chemical synthesis, N-(2-Hydroxyethyl)dodecanamide plays a crucial role in reactions where amide bonds are involved. Its hydroxyethyl group provides a site for potential modifications and functionalizations, making it a valuable building block for creating tailor-made molecules. By incorporating this compound into a synthesis pathway, chemists can introduce structural diversity and fine-tune the properties of the final product.Furthermore, N-(2-Hydroxyethyl)dodecanamide can act as a surfactant or emulsifier in certain reactions, promoting better dispersion of reactants and aiding in the formation of stable emulsions. This property is particularly advantageous in processes where immiscible substances need to be combined effectively.Overall, the application of N-(2-Hydroxyethyl)dodecanamide in chemical synthesis showcases its versatility and importance as a chemical reagent. Its strategic role in providing functional groups for molecular design and promoting efficient reactions makes it a valuable asset in the synthesis of various organic compounds.