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  2. Cinnamyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Cinnamyl_alcohol

    Cinnamyl alcohol or styron [2] is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves. It forms a white crystalline solid when pure, or a yellow oil when even slightly impure.

  3. Cinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Cinnamaldehyde

    Cinnamaldehyde is an organic compound with the formula C 9 H 8 O or C 6 H 6 CH=CHCHO.Occurring naturally as predominantly the trans isomer, it gives cinnamon its flavor and odor. [1] ...

  4. Phenylpropiolic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropiolic_acid

    Phenylpropiolic acid, C 6 H 5 CCCO 2 H, formed by the action of alcoholic potash on cinnamic acid dibromide, C 6 H 5 CHBrCHBrCO 2 H, crystallizes in long needles or prisms which melt at 136–137 °C. When heated with water to 120 °C, it yields phenylacetylene (C 6 H 5 CCH).

  5. Testosterone propionate/testosterone phenylpropionate ...

    en.wikipedia.org/wiki/Testosterone_propionate/...

    100 mg testosterone decanoate [1] Cumulatively, a 1 ml of the oil solution contains exactly 250 mg of above mentioned testosterone esters. [2] [3] This particular numerical value is clearly depicted in the name of the product, Sustanon 250. [4] They are provided as an oil solution and are administered by intramuscular injection. [5]

  6. Phenylpropanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanolamine

    [4] [6] [7] [5] About 4% of excreted material is in the form of metabolites. [4] The elimination half-life of immediate-release phenylpropanolamine is about 4 hours, with a range in different studies of 3.7 to 4.9 hours. [6] [7] [4] The half-life of extended-release phenylpropanolamine has ranged from 4.3 to 5.8 hours. [4]

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix "cyclo alkyl -" (e.g. "cyclohexyl-") or for benzene, "phenyl-".

  8. Phenylpropanoic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanoic_acid

    Phenylpropanoic acid can be prepared from cinnamic acid by hydrogenation. [5] [6] Originally it was prepared by reduction with sodium amalgam in water and by electrolysis.[7]A characteristic reaction of phenylpropanoic acid is its cyclization to 1-indanone.

  9. Testosterone phenylpropionate - Wikipedia

    en.wikipedia.org/wiki/Testosterone_phenylpropionate

    Testosterone phenylpropionate (BAN Tooltip British Approved Name; TPP) (brand name Testolent), or testosterone phenpropionate, also known as testosterone hydrocinnamate, is a synthetic anabolic-androgenic steroid (AAS) and an androgen ester – specifically, the C17β phenyl propionate ester of testosterone – which was formerly marketed in Romania.