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D8022-5G
Sigma-Aldrich
3,5-Dichlorophenyldiazonium tetrafluoroborate (C15-1233-416)
Price: $266.68List Price: $296.31Application Reactant for: Electron transfer chemistry Microwave-accelerated cross-coupling reactions Sandmeyer bromination for preparation of bromobenzene derivatives Catalytic thiocyanation in the presence of copper salts Electrochemical reduction -
290173-5GThe 19 F{′H} spectra of 3,5-difluorobenzaldehyde at low temperature in dimethyl ether solution was studied .
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290203-5GThe vibrational wavenumbers, geometry and various thermodynamic parameters were studied for 3,5-difluorobenzonitrile .
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290254-25GApplication 3,5-Difluorobenzoyl chloride was used in the synthesis of AMPA (α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) potentiator LY450108-[ 14 C] containing 14 C-label attached to the chiral center of the molecule .
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290254-5GApplication 3,5-Difluorobenzoyl chloride was used in the synthesis of AMPA (α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) potentiator LY450108-[ 14 C] containing 14 C-label attached to the chiral center of the molecule .
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469351-1GApplication 3,5-Difluorobenzylamine (DFBA) has been used as a derivatization reagent in the following studies: Determination of epichlorohydrin (ECH) in water by GC/MS analysis in selected ion monitoring (SIM) mode. Analysis of the epoxides
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469351-5GApplication 3,5-Difluorobenzylamine (DFBA) has been used as a derivatization reagent in the following studies: Determination of epichlorohydrin (ECH) in water by GC/MS analysis in selected ion monitoring (SIM) mode. Analysis of the epoxides
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197572-10G3,5-Difluorophenol
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197572-1G3,5-Difluorophenol
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471925-25GApplication Reactant involved in: Synthesis of honokiol analogs as angiogenesis inhibitors Homo-coupling reactions Suzuki-Miyaura cross-coupling reactions Enantioselective borane reduction of trifluoroacetophenone Other Notes Contains varying
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471925-5GApplication Reactant involved in: Synthesis of honokiol analogs as angiogenesis inhibitors Homo-coupling reactions Suzuki-Miyaura cross-coupling reactions Enantioselective borane reduction of trifluoroacetophenone Other Notes Contains varying
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579262-5G3,5-Dimethoxyphenyl trifluoromethanesulfonate