102-25-0 | 1,3,5-Triethylbenzene

Packsize	Purity	Availability	Price	Discounted Price
5g	94%	in stock	$5.00	$4.00
25g	94%	in stock	$12.00	$9.00

Description

• Catalog Number: AA07857
• Chemical Name: 1,3,5-Triethylbenzene
• CAS Number: 102-25-0
• Molecular Formula: C12H18
• Molecular Weight: 162.2713
• MDL Number: MFCD00009261
• SMILES: CCc1cc(CC)cc(c1)CC
• NSC Number: 406584

Computed Properties

• Complexity: 81.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Rotatable Bond Count: 3
• XLogP3: 4.3

Upstream Synthesis Route

1,3,5-Triethylbenzene, also known as sym-triethylbenzene, is a versatile organic compound commonly used in chemical synthesis. Its unique structure, characterized by three ethyl groups attached to a benzene ring, lends itself well to a variety of reactions and transformations in the laboratory.In chemical synthesis, 1,3,5-triethylbenzene is often employed as a starting material or intermediate in the preparation of other organic compounds. Its three ethyl groups provide convenient points of functionalization, allowing chemists to introduce different substituents or modify the molecule to create new, more complex structures. This compound can undergo various reactions such as Friedel-Crafts alkylation, oxidation, hydrogenation, and more, enabling the synthesis of a wide range of organic molecules with diverse properties and applications.Furthermore, 1,3,5-triethylbenzene can serve as a building block for the construction of aromatic compounds, polymers, pharmaceuticals, and agrochemicals. Its structural flexibility and reactivity make it a valuable tool in the hands of synthetic chemists seeking to design and produce novel materials with specific functions or properties.Overall, the application of 1,3,5-triethylbenzene in chemical synthesis highlights its importance as a key reagent for the creation of new organic molecules and the advancement of modern chemistry.

Literature

• Dicarboxylate recognition by two macrobicyclic receptors: selectivity for fumarate over maleate.

  The Journal of organic chemistry 20120518

• (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.

  Beilstein journal of organic chemistry 20120101

• Targeting HIV entry through interaction with envelope glycoprotein 120 (gp120): synthesis and antiviral evaluation of 1,3,5-triazines with aromatic amino acids.

  Journal of medicinal chemistry 20110811

• 4-Chloro-2',4',6'-triethyl-benzophenone: a redetermination.

  Acta crystallographica. Section E, Structure reports online 20110401

• Selective recognition of tetrahedral dianions by a hexaaza cryptand receptor.

  Organic & biomolecular chemistry 20091121

• Poly[[{μ(3)-tris-[2-(4-phenyl-1,2,3-triazol-1-yl)eth-yl]amine}silver(I)] hexa-fluorido-phosphate].

  Acta crystallographica. Section E, Structure reports online 20081001

• Syntheses of novel di- and trinucleating ligands having a triethylbenzene core with N,N-bidentate tethers: their complexation toward Pd and Rh organometallic fragments.

  Dalton transactions (Cambridge, England : 2003) 20080414

• A tricatecholic receptor for carbohydrate recognition: synthesis and binding studies.

  The Journal of organic chemistry 20070511

• Modeling the mononuclear, dinuclear, and trinuclear copper(I) reaction centers of copper proteins using pyridylalkylamine ligands connected to 1,3,5-triethylbenzene spacer.

  Inorganic chemistry 20061225

• New efficient organic activators for highly enantioselective reduction of aromatic ketones by trichlorosilane.

  Organic letters 20060817

• Formation of tetra(ethylene oxide) terminated Si-C linked monolayers and their derivatization with glycine: an example of a generic strategy for the immobilization of biomolecules on silicon.

  Langmuir : the ACS journal of surfaces and colloids 20051108

• Structure and photoluminescence property of two-dimensional coordination polymer complexes involving Cu(I)(6)X(6)(X = Cl, Br, I) hexagon prism cluster supported by a tripodal tripyridine ligand with 1,3,5-triethylbenzene spacer.

  Dalton transactions (Cambridge, England : 2003) 20051007

• Adsorption of single-ring organic compounds to wood charcoals prepared under different thermochemical conditions.

  Environmental science & technology 20050601

• A new tripodal receptor for molecular recognition of monosaccharides. A paradigm for assessing glycoside binding affinities and selectivities by 1H NMR spectroscopy.

  Journal of the American Chemical Society 20041222

• Molecular recognition of carbohydrates with acyclic pyridine-based receptors.

  The Journal of organic chemistry 20041029

• Supramolecular and coordination polymer complexes supported by a tripodal tripyridine ligand containing a 1,3,5-triethylbenzene spacer.

  Inorganic chemistry 20040726

• Tris(arylmethyl) derivatives of 1,3,5-trimethoxy- and 1,3,5-triethylbenzene.

  The Journal of organic chemistry 20030502