4-(Trifluoromethoxy)phenylboronic acid is a boronic acid derivative frequently employed as a research compound in organic synthesis. Its structure features an aromatic ring with a trifluoromethoxy substituent, contributing to its reactivity and utility in building complex molecules.
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4-Nitrophenylboronic acid
research compound
2,3,4,5-Tetrafluorobenzoic acid
research compound
4-Trifluoromethylphenylboronic acid
research compound
[3-Formyl-4-(trifluoromethoxy)phenyl]boronic acid
research compound
Sensitizer
research compound
Azido-PEG2-PFP ester
research compound
4,7,10,13,16-Pentaoxanonadec-18-ynoic acid, 2,5-dioxo-1-pyrrolidinyl ester
research compound
(5-Chloro-3-(trifluoromethyl)pyridin-2-yl)methanamine
research compound
The international HS code for 4-(Trifluoromethoxy)phenylboronic acid (CAS 139301-27-2) is 2931.90.
2931.90
2931 90 00
Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.
[4-(trifluoromethoxy)phenyl]boronic acid
HUOFUOCSQCYFPW-UHFFFAOYSA-N
B(C1=CC=C(C=C1)OC(F)(F)F)(O)O
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