1459737-08-6

Basic information

• Product Name: (4-(decylcarbamoyl)phenyl)boronic acid
• Synonyms: (4-(decylcarbamoyl)phenyl)boronic acid
• CAS NO: 1459737-08-6
• Molecular Weight: 305.225
• Mol File: 1459737-08-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-(decylcarbamoyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(decylcarbamoyl)phenyl)boronic acid(1459737-08-6)
• EPA Substance Registry System: (4-(decylcarbamoyl)phenyl)boronic acid(1459737-08-6)

Safety Data

• Hazardous Substances Data: 1459737-08-6(Hazardous Substances Data)

Upstream product

• 36043-57-9 2-decylisoindoline-1,3-dione 
• 2016-57-1 1-aminodecane 
• 14047-29-1 4-carboxyphenylboronic acid 

Downstream Products

• 1459737-07-5 4,4'-(1-decyl-1H-phenanthro[1,10,9,8-cdefg]carbazole-3,10-diyl)bis(N-decylbenzamide) 

Relevant articles and documents

Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers

A detailed investigation of the hierarchy of asymmetry operating in the self-assembly of achiral (1) and chiral ((S)-2 and (R)-3) 1,3,5-triphenylbenzenetricarboxamides (TPBAs) is reported. The aggregation of these TPBAs is conditioned by the point chirality at the peripheral side chains for (S)-2 and (R)-3. An efficient helix-to-helix interaction that goes further in the organization of fibrillar bundles is experimentally detected and theoretically supported only for the achiral TPBA 1. The effective interdigitation of the achiral aliphatic side chains produces a social self-sorting to form preferentially heterochiral macromolecular aggregates.

Luminescent and conductive supramolecular polymers obtained from an N-annulated perylenedicarboxamide

The tunable luminescent features along with the electrical conductivity (～2 × 10-4 S m-1) exhibited by the gel fibers formed through supramolecular polymerisation of the N-annulated perylenedicarboxamide based π-gelator 1 are reported.