1609930-04-2

Basic information

• Product Name: 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
• CAS NO: 1609930-04-2
• Molecular Weight: 1397.22
• Mol File: 1609930-04-2.mol

Chemical Properties

• CAS DataBase Reference: 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(CAS DataBase Reference)
• NIST Chemistry Reference: 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(1609930-04-2)
• EPA Substance Registry System: 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(1609930-04-2)

Safety Data

• Hazardous Substances Data: 1609930-04-2(Hazardous Substances Data)

Upstream product

• 931-53-3 Cyclohexyl isocyanide 
• 1609930-03-1 24-(t-butylcarbamoyl)-41-(cyclohexylamino)-8-(dec-9-en-1-yl)-7,10,26,41-tetraoxo-9,25-dioxa-13,29-dithia-6-azahentetracontan-40-yl stearate 
• 107-96-0 3-mercaptopropionic acid 
• 1609930-15-5 1-(cyclohexylamino)-1-oxododec-11-en-2-yl stearate 
• 1609930-00-8 3-((12-(cyclohexylamino)-12-oxo-11-(stearoyloxy)dodecyl)thio)propanoic acid 
• 1609930-01-9 12-((3-((1-(t-butylamino)-1-oxododec-11-en-2-yl)oxy)-3-oxopropyl)thio)-1-(cyclohexylamino)-1-oxododecan-2-yl stearate 
• 57-11-4 stearic acid 
• 112-45-8 10-Undecenal 

Downstream Products

• 1609930-05-3 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 

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