20138-27-6

Basic information

• Product Name: Hexadecanamide, N-[2-(2-hydroxyethoxy)ethyl]-
• CAS NO: 20138-27-6
• Molecular Formula: C20H41NO3
• Molecular Weight: 343.55
• Mol File: 20138-27-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Hexadecanamide, N-[2-(2-hydroxyethoxy)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Hexadecanamide, N-[2-(2-hydroxyethoxy)ethyl]-(20138-27-6)
• EPA Substance Registry System: Hexadecanamide, N-[2-(2-hydroxyethoxy)ethyl]-(20138-27-6)

Safety Data

• Hazardous Substances Data: 20138-27-6(Hazardous Substances Data)

Upstream product

• 929-06-6 2-(2-Aminoethoxy)ethanol 
• 112-67-4 n-hexadecanoyl chloride 
• 57-10-3 1-hexadecylcarboxylic acid 
• 74058-64-3 1-(2-Thioxo-thiazolidin-3-yl)-hexadecan-1-one 

Downstream Products

• 66654-00-0 2-(2-palmitamidoethoxy)acetic acid 

Relevant articles and documents

DNA CONTROLLED ASSEMBLY OF LIPID MEMBRANES

The present invention relates to detection of target nucleic acids by target nucleic acid induced liposome assembly. The invention provides oligonucleotides for use in detection and a method of detecting target nucleic acids. Other aspects of the invention are use of the oligonucleotide of the invention for detection, a kit for detection, a method of treatment comprising administrating the oligonucleotide of the invention and a pharmaceutical composition comprising the oligonucleotide of the invention.

DNA CONTROLLED ASSEMBLY OF LIPID MEMBRANES

The present invention relates to detection of target nucleic acids by targetnucleic acid induced liposome assembly. The invention provides oligonucleotides for use in detection and a method of detecting target nucleic acids.Other aspects of the invention

MONITORED AMINOLYSIS OF 3-ACYLTHIAZOLIDINE-2-THIONE : A NEW CONVENIENT SYNTHESIS OF AMIDE

3-Acylthiazolidine-2-thiones (1) were easily prepared and they were treated with several amines in dichloromethane to give amides 4 in very high yields within a short time.Aminoalcohols and aminophenols were selectively converted into acylaminoalcohols and acylaminophenols, respectively, by this reaction.One can monitor the reaction by disappearance of the yellow color of the starting material 1.Some amide alkaloids (15-18) have effectively been synthesized.