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Halo Compounds

Aryl and alkyl halides used as the electrophile. Bromides and iodides are the ones that couple under Suzuki-Miyaura and Buchwald-Hartwig conditions; chlorides are more often used for halogen-metal exchange or for straight substitution. Where the halide sits on an sp3 carbon, substitution and elimination compete and the temperature of the step decides which one wins. Trifluoromethyl and difluoromethyl entries are in this group as well.

16 catalogue entries group halo-compounds Typical use: Suzuki · Buchwald-Hartwig · Halogen-metal exchange
CASCompoundFormulaMWPackingQuote
65864-64-4(Difluoromethyl)trimethylsilaneC4H10F2Si124.201kg / 25kg / 100kgRequest
5009-31-4(Z)-1-Bromohex-3-eneC6H11Br163.061kg / 25kg / 100kgRequest
1535-67-7[(Difluoromethyl)thio]benzeneC7H6F2S160.191kg / 25kg / 100kgRequest
626-88-01-Bromo-4-MethylpentaneC6H13Br165.071kg / 25kg / 100kgRequest
35354-37-11-Bromo-5-MethylhexaneC7H15Br179.101kg / 25kg / 100kgRequest
53463-68-610-Bromo-1-decanolC10H21BrO237.181kg / 25kg / 100kgRequest
1611-56-911-Bromo-1-undecanolC11H23BrO251.201kg / 25kg / 100kgRequest
31608-22-72-(4-Bromobutoxy)tetrahydro-2H-pyranC9H17BrO2237.131kg / 25kg / 100kgRequest
2077-19-22-(4-bromophenyl)propan-2-olC9H11BrO215.091kg / 25kg / 100kgRequest
59772-49-52-Bromo-6-chloroanilineC6H5BrClN206.471kg / 25kg / 100kgRequest
21172-41-83-(3-(Trifluoromethyl)phenyl)propanalC10H9F3O202.171kg / 25kg / 100kgRequest
2968-33-43,3,3-Trifluoropropylamine hydrochlorideC3H7ClF3N149.541kg / 25kg / 100kgRequest
589-06-04-(4-Fluorophenyl)butanoic acidC10H11FO2182.191kg / 25kg / 100kgRequest
13991-36-14-Bromocrotonic acidC4H5BrO2164.991kg / 25kg / 100kgRequest
34714-00-66-chlorohexoxy(trimethyl)silaneC9H21ClOSi208.801kg / 25kg / 100kgRequest
88738-78-7Bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonateC7H9F6O5P318.111kg / 25kg / 100kgRequest
Entries are listed alphabetically. Packing is the standard unit weight; other quantities are quoted per lot.
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Halo Compounds outside the catalogue

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Group: Halo Compounds

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