unsubstituted

  • 31Ofloxacin — Systematic (IUPAC) name (RS) 7 fluoro 2 methyl 6 (4 methylpiperazin 1 yl) 10 oxo 4 oxa 1 azatricyclo[7.3.1.05,13]trideca 5(13),6,8,11 tetraene 11 carboxylic acid Clinical data …

    Wikipedia

  • 32Isoquinoline — Chembox new Name = Isoquinoline ImageFile = Isoquinoline chemical structure.png ImageSize = 450px ImageName = Chemical structure of Isoquinoline IUPACName = Isoquinoline OtherNames = benzo [c] pyridine, 2 benzanine Section1 = Chembox Identifiers… …

    Wikipedia

  • 33Dimethylformamide — N,N Dimethylformamide IUPAC na …

    Wikipedia

  • 34Quinacridone — Chembox new Name = Quinacridone ImageFile = Chinacridon.svg ImageName = IUPACName = 5,12 Dihydro quino [2,3 b] acridine 7,14 dione OtherNames = C.I.: 73900, Pigment Violet 19 Section1 = Chembox Identifiers SMILES… …

    Wikipedia

  • 35Thiourea — Chembox new ImageFile=thiourea.png ImageSize= ImageFile2=Thiourea 3D vdW.png IUPACName=thiourea OtherNames= Section1= Chembox Identifiers CASNo=62 56 6 PubChem=2723790 SMILES=C(=S)(N)N Section2= Chembox Properties Formula=CH4N2S MolarMass=76.1219 …

    Wikipedia

  • 36Trimethoxyamphetamine — TMAs, also known as trimethoxyamphetamines, are a family of isomeric psychedelic hallucinogenic drugs. There exist six different TMAs that differ only in the position of the three methoxy groups: TMA, TMA 2, TMA 3, TMA 4, TMA 5, and TMA 6. The… …

    Wikipedia

  • 37Biphenyl — IUPAC name …

    Wikipedia

  • 38Mass-independent fractionation — Mass independent (isotope) fractionation refers to any chemical or physical process that acts to separate isotopes, where the amount of separation does not scale in proportion with the difference in the masses of the isotopes. Most isotopic… …

    Wikipedia

  • 39Heptazine — Generic heptazine; R1, R2, R3 are arbitrary substituents. A heptazine, or tri s triazine or cyamelurine, is a type of chemical compound that consist of a planar triangular core group, C6N7, or three fused triazine rings, with three substituents… …

    Wikipedia

  • 40Madelung synthesis — The Madelung synthesis is a chemical reaction that produces (substituted or unsubstituted) indoles by the intramolecular cyclization of N phenylamides using strong base at high temperature.This method is essentially confined to the preparation of …

    Wikipedia