|Related Categories||Arenes, Building Blocks, Chemical Synthesis, Organic Building Blocks|
|density||0.862 g/mL at 25 °C(lit.)|
5, 25 g in glass bottle
1,3,5-Triethylbenzene was used as a supramoelcular template to organize molecular-recognition elements1. It was also used to synthesize a series of di- and trinucleating ligands2.
Certificate of Analysis
|Precautionary statements||P305 + P351 + P338|
|Personal Protective Equipment||Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter|
|Hazard Codes (Europe)||Xi|
|Risk Statements (Europe)||36/38|
|Safety Statements (Europe)||26|
|RIDADR||UN 3082 9 / PGIII|
|Flash Point(F)||168.8 °F|
|Flash Point(C)||76 °C|
1. (How) does 1,3,5-triethylbenzene scaffolding work? Analyzing the abilities of 1,3,5-triethylbenzene- and 1,3,5-trimethylbenzene-based scaffolds to preorganize the binding elements of supramolecular hosts and to improve binding of targets. Wang X and Hof F Beilstein J. Org. Chem. 8, 1-10, (2012)
2. Syntheses of novel di- and trinucleating ligands having a triethylbenzene core with N,N-bidentate tethers: their complexation toward Pd and Rh organometallic fragments. Higashihara G, Inagaki A, and Akita M Dalton Trans. (14), 1888-98, (2008)
Aldrich MSDS 1, 1750:A / Corp MSDS 1 (2), 3429:B / FT-IR 2 (2), 1640:A / FT-IR 1 (1), 942:D / FT-NMR 1 (2), 19:A / IR-Spectra (2), 505:D / IR-Spectra (3), 567:E / NMR-Reference 2 (1), 745:C / RegBook 1 (1), 1137:C / Structure Index 1, 175:D:4 / Vapor Phase 3, 863:B
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