Tolyl groups are aryl groups which are commonly found in the structure of diverse chemical compounds. They are considered nonpolar and hydrophobic groups. The functionalization to include tolyl groups into compounds is often done by Williamson etherification, using tolyl alcohols as reagents, or by C-C coupling reactions.

Apr 29, 2024 · o-tolyl-phenyl-methanol - cas 5472-13-9, synthesis, structure, density, melting point, boiling point

o-tolyl group Definition A group derived from toluene by removal of a hydrogen atom from the ring carbon atom at the 2-position.

Tris(o-tolyl)phosphine is an organophosphorus compound with the formula P(C 6 H 4 CH 3) 3. It is a white, water-insoluble solid that is soluble in organic solvents. In solution it slowly converts to the phosphine oxide. As a phosphine ligand, it has a wide cone angle of 194°.

Tri(o-tolyl)phosphine 97%; CAS Number: 6163-58-2; EC Number: 228-193-9; Synonyms: P(o-tol)3,Tris(o-tolyl)phosphine; Linear Formula: (CH3C6H4)3P at Sigma-Aldrich

In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos[nb 1]) is a univalent functional group with the chemical formula −SO2−C6H4−CH3. It consists of a tolyl group, −C6H4−CH3, joined to a sulfonyl group, −SO2−, with the open valence on sulfur.

Sep 1, 2008 · The reaction of the furoyl isothiocyanate with o-toluidine in dry acetone yielded the title compound, N-(o-tolyl) thiourea, as a secondary product (Fig. 1). The title molecule is present in the thioamide form and it is a typical N-monosubstituted thiourea derivative with usual geometric parameters.

Mar 26, 2024 · On occasion o -Tol about the ortho isomer, for instance P(o-tol)X3 P (o - t o l) X 3 for tris (o -tolyl)phosphine ligand (or as P(o-Tol)X3 P (o - T o l) X 3), too) though this arguably appears more often in figure / table captions to shorten line formulae, than in structure formulae.

May 1, 2015 · The synthesis and catalytic activity of [(TMEDA)Ni(o-tolyl)Cl], an air-stable, crystalline solid, is described. This complex is an effective precatalyst in a variety of nickel-catalyzed transformations.

2-methylphenyl isothiocyanate, o-tolyl isothiocyanate, 2-tolyl isothiocyanate, o-tolylisothiocyanate, benzene, 1-isothiocyanato-2-methyl, 1-isothiocyanato-2-methyl-benzene, 2-methylphenylisothiocyanate, isothiocyanic acid o-tolyl ester, isothiocyanic acid, o-tolyl ester, 2-methylbenzenisothiocyanate: PubChem CID: 69195: IUPAC Name