Thiobenzophenone is an organosulfur compound with the formula (C6H5)2CS. It is the prototypical thioketone. Unlike other thioketones that tend to dimerize...

is produced so from allicin. Another route is oxidation, as with thiobenzophenone from diphenylsulfine: (C6H5)2C=S + [O] → (C6H5)2C=S=O Sulfene - related...

-thioyl- (-CSR') or sulfanylidene- (=S) -thione Diphenylmethanethione (Thiobenzophenone) Thial Carbonothioyl RCSH methanethioyl- (-CSH) or sulfanylidene- (=S)...

BA; Kane-Barber, JM; O'Reilly, RJ; Shi, L (2007). "Polymer-supported thiobenzophenone : a self-indicating traceless 'catch and release' linker for the synthesis...

alkylthioketones typically tend to form polymers or rings. The C=S bond length of thiobenzophenone is 1.63 Å, which is comparable to 1.64 Å, the C=S bond length of thioformaldehyde...

induce vomiting, and be detected over long distances.[citation needed] Thiobenzophenone, a thioketone that can be isolated as a solid Bromoacetone Chloroacetone...

(RC(=S)R′) are uncommon with alkyl substituents, but one example is thiobenzophenone. Thioaldehydes are rarer still, reflecting their lack of steric protection...

the C-S bond by C-N pi-bonding is indicated by the short C=S bond in thiobenzophenone, which is 1.63 Å. Thiourea occurs in two tautomeric forms, of which...

C13H10S (molar mass: 198.28 g/mol, exact mass: 198.0503 u) may refer to: Thiobenzophenone Thioxanthene This set index page lists chemical structure articles...