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used as a pigment and as a precursor to other manganese compounds; used as a reagent in organic synthesis for the oxidation of allylic alcohols Meta-Chloroperoxybenzoic acid: used as an oxidant in organic synthesis Methyl tert-butyl ether: a gasoline additive; also used in organic chemistry as a relatively inexpensive solvent Millon's reagent
Download QR code; Print/export ... Well-known reactions and reagents in organic chemistry include ... List of organic compounds;
This category was created to provide a "home" for inorganic compounds (such as NaBH 4) that are widely used in stoichiometric quantities in organic chemistry, but widely used organic reagents (such as oxalyl chloride) may belong here also. This category is not for catalysts such as Pd.
NIST Chemistry Webbook National Institute of Standards and Technology: spectra CAS ionization energy mass spectrum, InChI C+CAS "NIST Webbook". NMRShiftDB University of Cologne: organic nuclear magnetic resonance spectra "NMRShiftDB". 43,581 NORMAN SLE NORMAN Suspect List Exchange environmental monitoring "NORMAN SLE". 110,000 OMG
Triethyloxonium tetrafluoroborate is the organic oxonium compound with the formula [(CH 3 CH 2) 3 O] + [BF 4] −. It is often called Meerwein's reagent or Meerwein's salt after its discoverer Hans Meerwein. [2] [3] Also well known and commercially available is the related trimethyloxonium tetrafluoroborate. The compounds are white solids that ...
Download QR code; Print/export ... The TASF reagent or tris ... sulfonium difluorotrimethylsilicate is a reagent in organic chemistry with structural formula [ ...
The reaction is carried out in an ice bath, and the reagents are added dropwise so that the temperature does not rise above 20 °C. Diethyl hydrazodicarboxylate is a solid with melting temperature of 131–133 °C which is collected as a residue; it is significantly more stable to heating than DEAD and is conventionally dried at a temperature ...
The sulfonation of hydroxylamine can also be effected with chlorosulfonic acid [3] by a method first published in 1925 [7] and refined for Organic Syntheses. [ 8 ] The hydroxylamine- O -sulfonic acid, which should be stored at 0 °C to prevent decomposition, can be checked by iodometric titration.