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About This Item
Linear Formula:
CF3C6H4B(OH)2
CAS Number:
Molecular Weight:
189.93
Beilstein:
3544189
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.22
Quality Level
분석
≥95.0%
mp
245-250 °C (lit.)
작용기
fluoro
SMILES string
OB(O)c1ccc(cc1)C(F)(F)F
InChI
1S/C7H6BF3O2/c9-7(10,11)5-1-3-6(4-2-5)8(12)13/h1-4,12-13H
InChI key
ALMFIOZYDASRRC-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
4-(Trifluoromethyl)phenylboronic acid can be used as a reactant in:
It can also be used as a reactant to prepare:
- Site-selective Suzuki-Miyaura cross-coupling reactions.
- Palladium-catalyzed direct arylation reactions.
- Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence.
- Ruthenium catalyzed direct arylation.
- Ligand-free copper-catalyzed coupling reactions.
- Amination and conjugate addition reactions.
- Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.
- Rhodium-catalyzed asymmetric 1,4-addition reactions.
- Copper-catalyzed nitration reactions.
- Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation.
- Palladium catalyzed allylation reaction with allyl alcohols.
- N-Arylation of imidazoles and amines in the presence of copper-exchanged fluorapatite as a catalyst.
It can also be used as a reactant to prepare:
- Thiazole derivatives for printable electronics.
- Terphenyl benzimidazoles as tubulin polymerization inhibitors.
- Aryl ketones by cross-coupling reaction with acid chlorides.
기타 정보
Contains varying amounts of anhydride
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
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