方案
98%
mp
100-102 °C (lit.)
官能团
amide
SMILES字符串
CCCCCC(N)=O
InChI
1S/C6H13NO/c1-2-3-4-5-6(7)8/h2-5H2,1H3,(H2,7,8)
InChI key
ALBYIUDWACNRRB-UHFFFAOYSA-N
一般描述
Hexanoamide is the most rapidly hydrolysed substrate for amidase from Aspergillus nidulans. Zirconium mediated conversion of hexanoamide to hexanenitrile has been reported.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Jyoti Choithani et al.
Analytical biochemistry, 357(2), 240-248 (2006-08-26)
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 function undergoes conjugate addition to 3'- or 5'-thiol-modified oligonucleotides. The construction of microarrays
Alexandra Thomas et al.
Cancers, 12(8) (2020-08-23)
Pancreatic cancer remains a recalcitrant neoplasm associated with chemoresistance and high fatality. Because it is frequently resistant to apoptosis, exploiting autophagic cell death could offer a new treatment approach. We repurpose echinomycin, an antibiotic encapsulated within a syndecan-1 actively targeted
Jianfei Zheng et al.
Bioconjugate chemistry, 19(6), 1227-1234 (2008-05-30)
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 ligand conjugates that target the nuclear thyroid
Aliphatic and enantioselective amidases: from hydrolysis to acyl transfer activity.
D Fournand et al.
Journal of applied microbiology, 91(3), 381-393 (2001-09-15)
Preparation and characterization of galactose-modified liposomes by a nonaqueous enzymatic reaction.
Bo-hong Guo et al.
Journal of liposome research, 21(3), 255-260 (2011-05-07)
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-loaded liposome (GA-LP) and glycyrrhetinic-acid-loaded liposome surface modified with galactose (NOH-GA-LP) were prepared by the
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