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nicergoline (27848-84-6)  
Nicergolin neuraxpharm  ·  ergobel  ·  Krewel Brand of Nicergoline
Nicergoline (INN, marketed under the trade name Sermion) is an ergot derivative used to treat senile dementia and other disorders with vascular origins. It decreases vascular resistance and increases arterial blood flow in the brain, improving the utilization of oxygen and glucose by brain cells. It has similar vasoactive properties in other areas of the body, particularly the lungs.

Related Results:
Diphenyl oxide (101-84-8)  
phenyl ether  ·  diphenyl ether
Diphenyl ether is the organic compound with the formula O(C6H5)2. The molecule is subject to reactions typical of other phenyl rings, including hydroxylation, nitration, halogenation, sulfonation, and Friedel–Crafts alkylation or acylation. This simple diaryl ether enjoys a variety of niche applications.
Diphenyl phosphoramidate (2015-56-7)  
amidophosphoric acid, diphenyl ester
Diphenylmethanol (91-01-0)  
benzhydrol  ·  benzohydrol  ·  dicyclohexylmethanol
Diphenylmethanol, (C6H5)2CHOH (also known as benzhydrol), is a secondary alcohol with a relative molecular mass of 184.23 g/mol. It has a melting point of 69 °C and a boiling point of 298 °C. It has uses in perfume and pharmaceutical manufacture.
Biphenyl (92-52-4, 68409-73-4)  
diphenyl  ·  diphenyl, 14C-labeled
Biphenyl (or diphenyl or phenylbenzene or 1,1′-biphenyl or lemonene) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl. It has a distinctively pleasant smell.
Diphenyl sulfone (127-63-9)  
Diphenyl sulfone is an organosulfur compound with the formula (C6H5)2SO2. It is a white solid that is soluble in organic solvents. It is used as a high temperature solvent.
Diphenyl chlorophosphate (2524-64-3)  
diphenylphosphorylchloridate
Diphenyl oxalate (3155-16-6)  
Diphenyl oxalate (trademark name Cyalume) is a solid ester whose oxidation products are responsible for the chemiluminescence in a glowstick. It can be synthesized by fully esterifying phenol with oxalic acid. The reaction with hydrogen peroxide that diphenyl oxalate undergoes produces phenol and 1,2-dioxetanedione, which excites the dye and releases a photon as it decomposes to carbon dioxide.
1,4-Diphenylbutadiyne (886-66-8)  
1,4-diphenylbutadiyne, ion (1+)  ·  1,4-DPB
Diphenyl diselenide (1666-13-3)  
diphenyldiselenide
Diphenyl diselenide is the chemical compound with the formula (C6H5)2Se2, abbreviated Ph2Se2 This orange-coloured solid is the oxidized derivative of benzeneselenol. It is used as a source of the PhSe unit in organic synthesis. Ph2Se2 is prepared by the oxidation of benzeneselenoate, the conjugate base of benzeneselenol which is generated via the Grignard reagent: PhMgBr + Se → PhSeMgBr 2 PhSeMgBr + Br2 → Ph2Se2 + 2 MgBr2 The molecule has idealized C2-symmetry, like hydrogen peroxide and related molecules.
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