4-Trifluoromethylphenylboronic acid

Modify Date: 2024-01-01 22:05:41

4-Trifluoromethylphenylboronic acid Structure
4-Trifluoromethylphenylboronic acid structure
Common Name 4-Trifluoromethylphenylboronic acid
CAS Number 128796-39-4 Molecular Weight 189.93
Density 1.4±0.1 g/cm3 Boiling Point 258.6±50.0 °C at 760 mmHg
Molecular Formula C7H6BF3O2 Melting Point 245-250 °C(lit.)
MSDS Chinese USA Flash Point 110.2±30.1 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 4-Trifluoromethylphenylboronic acid


4-Trifluoromethylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 4-Trifluoromethylphenylboronic acid
Synonym More Synonyms

 4-Trifluoromethylphenylboronic acid Biological Activity

Description 4-Trifluoromethylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
In Vitro 4-Trifluoromethylphenylboronic acid 用于通过铜交换的氟磷灰石对咪唑和胺进行 N-芳基化,以及用于微波促进的与酰氯的交叉偶联,从而生成芳基酮。

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 258.6±50.0 °C at 760 mmHg
Melting Point 245-250 °C(lit.)
Molecular Formula C7H6BF3O2
Molecular Weight 189.93
Flash Point 110.2±30.1 °C
Exact Mass 190.041290
PSA 40.46000
LogP 2.16
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.462
Storage condition 0-6°C

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S37/39-S26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2931900090

 Synthetic Route

 Customs

HS Code 2931900090
Summary 2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

 Articles15

More Articles
Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.

Org. Lett. 7th ed., 14 , 1930-1933, (2012)

A Ru-catalyzed direct arylation of benzylic sp(3) carbons of acyclic amines with arylboronates is reported. This highly regioselective and efficient transformation can be performed with various combin...

Tandem-type Pd(II)-catalyzed oxidative Heck reaction/intramolecular C-H amidation sequence: a novel route to 4-aryl-2-quinolinones.

Chem. Commun. (Camb.) 36th ed., 48 , 4332-4334, (2012)

A novel catalytic method for synthesizing 4-aryl-2-quinolinones is reported. The process involves two mechanistically independent, sequential Pd(II)-catalyzed reactions--the oxidative Heck reaction an...

Combined experimental-theoretical NMR study on 2,5-bis(5-aryl-3-hexylthiophen-2-yl)-thiazolo[5,4-d]thiazole derivatives for printable electronics.

Magn. Reson. Chem. 5th ed., 50 , 379-387, (2012)

Four 2,5-bis(5-aryl-3-hexylthiophen-2-yl)thiazolo[5,4-d]thiazole derivatives have been synthesized and thoroughly characterized. The extended aromatic core of the molecules was designed to enhance the...

 Synonyms

QBQR DXFFF
MFCD00151855
4-(Trifluoromethyl)phenylboronic acid
Boronic acid, B-[4-(trifluoromethyl)phenyl]-
α,α,α-Trifluoro-p-tolueneboronic Acid,contains varying amounts of An
α,α,α-Trifluoro-p-tolueneboronic Acid
Dihydroxy[4-(trifluoromethyl)phenyl]borane
α,α,α-Trifluoro-p-tolylboronic acid
(4-(Trifluoromethyl)phenyl)boronic acid
4-(Trifluoromethyl)benzeneboronic acid
[4-(Trifluoromethyl)phenyl]boranediol
B-[4-(Trifluoromethyl)phenyl]boronic acid
[4-(Trifluoromethyl)phenyl]boronic acid
(4-Trifluoromethylphenyl)boronic acid