n-Hexanamide
n-Hexanamide structure
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Common Name | n-Hexanamide | ||
|---|---|---|---|---|
| CAS Number | 628-02-4 | Molecular Weight | 115.174 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 255.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C6H13NO | Melting Point | 100-102 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 102.2±18.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Zirconium-mediated conversion of amides to nitriles: a surprising additive effect.
Angew. Chem. Int. Ed. Engl. 43(40) , 5375-7, (2004)
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Aliphatic and enantioselective amidases: from hydrolysis to acyl transfer activity.
J. Appl. Microbiol. 91(3) , 381-93, (2001)
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Carcinogenesis bioassay of acetamide, hexanamide, adipamide, urea and P-tolylurea in mice and rats.
J. Environ. Pathol. Toxicol. 3(5-6) , 149-70, (1980) As a part of the National Cancer Institute's effort to screen environmental and occupational chemicals for chronic toxicity and carcinogenicity, the amides acetamide, hexanamide, adipamide, urea, and p-tolylurea were fed to male and female C57B1/6 mice and Fi... |
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Development of a thyroid hormone receptor targeting conjugate.
Bioconjug. Chem. 19(6) , 1227-34, (2008) Molecular conjugates of hormone receptor-ligands with molecular probes or functional domains are finding diverse applications in chemical biology. Whereas many examples of hormone conjugates that target steroid hormone receptors have been reported, practical ... |
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N-(3-Triethoxysilylpropyl)-6-(N-maleimido)-hexanamide: An efficient heterobifunctional reagent for the construction of oligonucleotide microarrays.
Anal. Biochem. 357(2) , 240-8, (2006) Synthesis of a new heterobifunctional reagent, N-(3-triethoxysilylpropyl)-6-(N-maleimido)-hexanamide (TPMH), for the preparation of oligonucleotide microarrays is described. Its triethoxysilyl function is specific toward virgin glass surface and maleimide fun... |
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Preparation and characterization of galactose-modified liposomes by a nonaqueous enzymatic reaction.
J. Liposome Res. 21(3) , 255-60, (2011) In this study, NOH (NOH = N-octadecyl-4-[(D-galactopyranosyl)oxy]-2,3,5,6-tetrahydroxy hexanamide) was enzymatically synthesized as a targeting molecule and incorporated into liposomes to prepare a liposome surface modified with galactose. Glycyrrhetinic-acid... |