Halogenated Heterocycles

tert-Butyl methyl(3-piperidinylmethyl)carbamate hydrochloride.

tert-Butyl[3-(trifluoromethylpyrrolidine-3-yl)]carbamate.

ApplicationTetrachlorothiophene was used in the preparation of 3,4,5-trichloro-2-thiophenecarbonyl chloride.Solvent for organic reactions and spectral use.

ApplicationTetrachlorothiophene was used in the preparation of 3,4,5-trichloro-2-thiophenecarbonyl chloride.Solvent for organic reactions and spectral use.

ApplicationTetrachlorothiophene was used in the preparation of 3,4,5-trichloro-2-thiophenecarbonyl chloride.Solvent for organic reactions and spectral use.

DescriptionTetradecafluorohexane in the gas phase reacts spontaneously with lithium amalgam, to give a solid and intimate mixture of lithium fluoride and elemental polymeric carbon with a small amount of superstoichiometric

DescriptionTetradecafluorohexane in the gas phase reacts spontaneously with lithium amalgam, to give a solid and intimate mixture of lithium fluoride and elemental polymeric carbon with a small amount of superstoichiometric

DescriptionTetradecafluorohexane in the gas phase reacts spontaneously with lithium amalgam, to give a solid and intimate mixture of lithium fluoride and elemental polymeric carbon with a small amount of superstoichiometric

Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η2-nitrile

Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η2-nitrile

Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η2-nitrile

Tetrahydro-2H-pyran-4-carbonyl chloride.