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4-(Trifluoromethyl)phenylboronic acid

CAS 128796-39-4CF3C6H4B(OH)2Chemical Synthesis

4-(Trifluoromethyl)phenylboronic acid (CAS: 128796-39-4, Formula: CF3C6H4B(OH)2, MW: 189.93) is a key organometallic reagent supplied by Tech Serve Solutions. This aryl boronic acid derivative is essential for various cross-coupling reactions, including Suzuki-Miyaura, palladium-catalyzed direct arylation, and rhodium-catalyzed asymmetric additions. Its utility spans organic synthesis, particularly in preparing complex molecules and intermediates for advanced chemical and pharmaceutical research.

IUPAC
α,α,α-Trifluoro-p-tolylboronic acid,4-(Trifluoromethyl)benzeneboronic acid,[p-(Trifluoromethyl)phenyl]boronic acid
Synonyms
α,α,α-Trifluoro-p-tolylboronic acid4-(Trifluoromethyl)benzeneboronic acid[p-(Trifluoromethyl)phenyl]boronic acid
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4-(Trifluoromethyl)phenylboronic acid (CF3C6H4B(OH)2) — chemical structure, CAS 128796-39-4; Chemistry, fine chemical supplied by Tech Serve Solutions
Aryl Boronic AcidsBoronic AcidsChemical Synthesis
01 /Applications

Suzuki-Miyaura Cross-Coupling Reactions

Utilised in site-selective and regioselective Suzuki-Miyaura cross-coupling reactions, a fundamental method for carbon-carbon bond formation. It is also employed in tandem palladium-catalyzed intramolecular aminocarbonylation and annulation sequences.

Palladium-Catalyzed Arylation and Heck Reactions

Serves as a crucial reagent in palladium-catalyzed direct arylation reactions and in tandem-type oxidative Heck reactions coupled with intramolecular C-H amidation sequences.

Ruthenium and Rhodium Catalysis

Applicable in ruthenium-catalyzed direct arylation and rhodium-catalyzed asymmetric 1,4-addition reactions, expanding its scope in stereoselective synthesis.

Copper-Catalyzed Transformations

Engaged in ligand-free copper-catalyzed coupling reactions, amination, conjugate addition reactions, and copper-catalyzed nitration reactions.

02 /Properties
Molecular weight189.93
Linear formulaCF3C6H4B(OH)2
Assay≥95.0%
ApplicationReagent used for• Site-selective Suzuki-Miyaura cross-coupling reactions1• Palladium-catalyzed direct arylation reactions2• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence3• Ruthenium catalyzed direct arylation4• Ligand-free copper-catalyzed coupling reactions5• Amination and conjugate addition reactions6• Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions7• Rhodium-catalyzed asymmetric 1,4-addition reactions8• Copper-catalyzed nitration reactions9• Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation10Reagent used in Preparation of• Thiazole deriv
Melting point245-250 °C(lit.)
03 /Safety & handling
GHS hazard pictogram: Harmful / irritant (GHS07)
Harmful / irritant
Warning

Hazard statements

  • H302Harmful if swallowed
Protective equipmentdust mask type N95 (US), Eyeshields, Gloves
Water hazard class (WGK, DE)3
Hazard codes (EU)Xn
Risk statements (R)22

Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.

04 /Identifiers & registry
CAS number
128796-39-4
MDL number
MFCD00151855
PubChem substance
24867498
Beilstein registry
3544189
05 /Quality & supply

Documentation

Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.

Supply & logistics

Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.

06 /Frequently asked questions

What is 4-(Trifluoromethyl)phenylboronic acid used for?

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4-(Trifluoromethyl)phenylboronic acid is a versatile reagent primarily used in various cross-coupling reactions such as Suzuki-Miyaura, palladium-catalyzed direct arylation, and Heck reactions. It also finds application in ruthenium and rhodium-catalyzed transformations, as well as copper-catalyzed coupling and nitration reactions.

What are the CAS number and formula for 4-(Trifluoromethyl)phenylboronic acid?

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The CAS number for 4-(Trifluoromethyl)phenylboronic acid is 128796-39-4, and its linear formula is CF3C6H4B(OH)2.

What grade and purity does Tech Serve Solutions supply?

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Tech Serve Solutions supplies 4-(Trifluoromethyl)phenylboronic acid with a minimum assay of ≥95.0%. This product is intended for laboratory and research use, and TSS does not represent it as USP, BP, or EP grade.

How should 4-(Trifluoromethyl)phenylboronic acid be handled safely?

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4-(Trifluoromethyl)phenylboronic acid is classified with GHS07 symbol and a 'Warning' signal word, presenting H302 hazard statement. Handle with appropriate personal protective equipment, including a dust mask type N95 (US), eyeshields, and gloves, in a well-ventilated area.

Is 4-(Trifluoromethyl)phenylboronic acid available for export?

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Yes, Tech Serve Solutions is a specialist global supplier and exporter of fine chemicals, including 4-(Trifluoromethyl)phenylboronic acid, and can fulfil international orders.

How can I request a quote or sample?

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To request a quote or a sample of 4-(Trifluoromethyl)phenylboronic acid, please contact the Tech Serve Solutions sales team via our website or your usual sales representative.

Need 4-(Trifluoromethyl)phenylboronic acid in a specific grade or volume?