1609930-05-3

Basic information

• Product Name: 39-(tert-butylcarbamoyl)-56-(cyclohexylamino)-7-(dec-9-en-1-yl)-6,9,25,41,56-pentaoxo-23-(pentylcarbamoyl)-8,24,40-trioxa-12,28,44-trithia-5-azahexapentacontan-55-yl stearate
• CAS NO: 1609930-05-3
• Molecular Weight: 1648.63
• Mol File: 1609930-05-3.mol

Chemical Properties

• CAS DataBase Reference: 39-(tert-butylcarbamoyl)-56-(cyclohexylamino)-7-(dec-9-en-1-yl)-6,9,25,41,56-pentaoxo-23-(pentylcarbamoyl)-8,24,40-trioxa-12,28,44-trithia-5-azahexapentacontan-55-yl stearate(CAS DataBase Reference)
• NIST Chemistry Reference: 39-(tert-butylcarbamoyl)-56-(cyclohexylamino)-7-(dec-9-en-1-yl)-6,9,25,41,56-pentaoxo-23-(pentylcarbamoyl)-8,24,40-trioxa-12,28,44-trithia-5-azahexapentacontan-55-yl stearate(1609930-05-3)
• EPA Substance Registry System: 39-(tert-butylcarbamoyl)-56-(cyclohexylamino)-7-(dec-9-en-1-yl)-6,9,25,41,56-pentaoxo-23-(pentylcarbamoyl)-8,24,40-trioxa-12,28,44-trithia-5-azahexapentacontan-55-yl stearate(1609930-05-3)

Safety Data

• Hazardous Substances Data: 1609930-05-3(Hazardous Substances Data)

Upstream product

• 112-45-8 10-Undecenal 
• 2769-64-4 n-butyl isonitrile 
• 1609930-04-2 5-((3-((12-(cyclohexylamino)-12-oxo-11-(stearoyloxy)dodecyl)thio)propanoyl)oxy)-2,2-dimethyl-4,19-dioxo-21-(pentylcarbamoyl)-20-oxa-16,32-dithia-3-azapentatriacontan-35-oic acid 

Relevant articles and documents

Sequence control in polymer chemistry through the Passerini three-component reaction

A new strategy to achieve sequence control in polymer chemistry based on the iterative application of the versatile Passerini three-component reaction (P-3CR) in combination with efficient thiol-ene addition reactions is introduced. First, stearic acid was used as a starting substrate to build up a sequence-defined tetramer with a molecular weight of 1.6 kDa. Using an acid-functionalized PEG allowed for an easier isolation of the sequence-defined macromolecules by simple precipitation and led to a sequence-defined pentamer in a block-copolymer architecture. Importantly, this new strategy completely avoids protecting group chemistry. By following this strategy, a different side chain can be introduced to the polymer/oligomer backbone in a simple way and at a defined position within the macromolecule. The iterative application of the Passerini three-component reaction and the thiol-ene addition reaction provides sequence-defined macromolecules without the utilization of any protecting group. Copyright