ChemicalBook > CAS DataBase List > 3,5-Bis(trifluoromethyl)benzeneboronic acid

3,5-Bis(trifluoromethyl)benzeneboronic acid

Product Name
3,5-Bis(trifluoromethyl)benzeneboronic acid
CAS No.
73852-19-4
Chemical Name
3,5-Bis(trifluoromethyl)benzeneboronic acid
Synonyms
3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC ACID;AKOS BRN-0072;RARECHEM AH PB 0029;3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC;3,5-Bis(trifluoroMethyl)benzeneboronic;5-Bis(trifluoroMethyl)phenylboronic acid;3,5-Bis(trifloroMethyl)phenylboronic acid;3,5-DI(TRIFLUOROMETHYL)PHENYLBORONIC ACID;3,5--TrifluoroMethyl benzene boronic acid;3,5-BIS(TRIFLUOROMETHYL)PHENYLBOROIC ACID
CBNumber
CB6205984
Molecular Formula
C8H5BF6O2
Formula Weight
257.93
MOL File
73852-19-4.mol
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3,5-Bis(trifluoromethyl)benzeneboronic acid Property

Melting point:
217-220 °C (lit.)
Boiling point:
248.1±50.0 °C(Predicted)
Density 
1.50±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
Crystals or Powder
pka
6.57±0.10(Predicted)
color 
White to light yellow
BRN 
7379990
InChI
InChI=1S/C8H5BF6O2/c10-7(11,12)4-1-5(8(13,14)15)3-6(2-4)9(16)17/h1-3,16-17H
InChIKey
BPTABBGLHGBJQR-UHFFFAOYSA-N
SMILES
B(C1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1)(O)O
CAS DataBase Reference
73852-19-4(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
WGK Germany 
3
TSCA 
No
HazardClass 
IRRITANT
HS Code 
29163990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
471070
Product name
3,5-Bis(trifluoromethyl)phenylboronic acid
Purity
≥95%
Packaging
5g
Price
$78.27
Updated
2025/07/31
TCI Chemical
Product number
B1886
Product name
3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)
Packaging
1g
Price
$21
Updated
2025/07/31
TCI Chemical
Product number
B1886
Product name
3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)
Packaging
5g
Price
$58
Updated
2025/07/31
TCI Chemical
Product number
B1886
Product name
3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)
Packaging
25g
Price
$172
Updated
2025/07/31
TRC
Product number
B412868
Product name
3,5-Bis(trifluoromethyl)phenylboronic acid
Packaging
5g
Price
$55
Updated
2021/12/16
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3,5-Bis(trifluoromethyl)benzeneboronic acid Chemical Properties,Usage,Production

Chemical Properties

Off-white Cryst

Uses

suzuki reaction

Uses

Reactant involved in the synthesis of:

  • Methylene-arylbutenones via carbonylative arylation of allenols
  • 4-aminoquinoline analogs via Ullman / Suzuki / Negishi coupling
  • Primary amino acid derivatives with anticonvulsant activity
  • Alkyl arylcarbamates via Cu-catalyzed coupling with potassium cyanate
  • Aryl-substituted succinimides and cyclic ketones by asymmetric conjugate addition
  • Axially chiral dicarboxylic acids for asymmetric Mannich-type reactions

Synthesis

121-43-7

328-70-1

7732-18-5

73852-19-4

General procedure for the synthesis of 3,5-bis(trifluoromethyl)benzeneboronic acid from trimethyl borate, 3,5-bis(trifluoromethyl)bromobenzene, and electrophoretic-grade water: in a three-necked, dry, round-bottomed flask equipped with a rod-shaped magnetic stirrer, a 500-ml dropping funnel, condenser tube, and nitrogen introduction tube, 9.30 g of magnesium flakes were added under nitrogen protection and 220 ml of tetrahydrofuran (THF), which had been distillate-purified, were added ). The temperature of the reaction system was maintained in the range of 0 to 5°C by means of an ice bath. At this temperature, 44.0 mL of 3,5-bis(trifluoromethyl)bromobenzene was slowly added through a dropping funnel and the addition process was controlled to be completed within 1 hour. After the addition was completed, the reaction was slowly warmed to room temperature and continued for 16 hours to obtain a dark brown viscous solution. Subsequently, the reaction solution was cooled to -70°C in a dry ice/acetone bath and 28.97 mL of trimethyl borate was slowly added dropwise through a dropping funnel. After completion of the dropwise addition, the reaction solution was allowed to warm naturally to room temperature and the reaction was continued for 12 hours to obtain a brown viscous solution. Under cooling in an ice bath, 144.5 ml of 37 wt% aqueous hydrochloric acid solution was mixed with 63.3 ml of distilled water and slowly added to the reaction solution over a period of 1 hour, after which the reaction was continued for 24 hours. Upon completion of the reaction, the red organic layer was separated using a partition funnel. The organic layer was concentrated under reduced pressure to remove the solvent and the solid residue obtained was purified by recrystallization in distilled water. The resulting white crystals were collected, washed with petroleum ether and dried at room temperature for 24 hours to afford the target product 3,5-bis(trifluoromethyl)benzeneboronic acid (6FBB) (19.44 g, yield: 85%).

References

[1] Patent: KR2015/112649, 2015, A. Location in patent: Paragraph 0089; 0093-0095

3,5-Bis(trifluoromethyl)benzeneboronic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 3,5-Bis(trifluoromethyl)benzeneboronic acid manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
3,5-Bis(trifluoromethyl)benzeneboronic acid 73852-19-4
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-10-25
Career Henan Chemical Co
Product
3,5-Bis(trifluoromethyl)benzeneboronic acid 73852-19-4
Price
US $1.00/KG
Min. Order
1KG
Purity
97%-99%
Supply Ability
100kg
Release date
2019-07-03

73852-19-4, 3,5-Bis(trifluoromethyl)benzeneboronic acidRelated Search:


  • RARECHEM AH PB 0029
  • 3,5-Bis(trifluoromethyl)benzeneboronic acid, 97+%
  • 3,5-Bis(trifluoromethyl)phenylboranic acid
  • Boric acid 3,5-bis(trifluoromethyl)phenyl ester
  • 3,5-Bis(trifluoromethyl)benzeneboronic acid,95%
  • 3,4-Bis(trifluoromethyl) phenylboronic acid
  • 5-Bis(trifluoroMethyl)phenylboronic acid
  • 3,5-Bis(trifloroMethyl)phenylboronic acid
  • 3,5-Bis(trifluoroMethyl)benzeneboronic acid, 95% 1GR
  • 3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC ACID(CONTAINS VARYING AMOUNTS OF ANHYDRIDE)
  • 3,5-Bis(trifluoromethyl)benzeneboronic acid, 99% [3,5-Bis(trifluoromethyl)phenylboronic acid]
  • 3,5-Bis(trifluoromethyl)benzeneboronic acid 98%
  • 3,5-Bis(trifluoromethyl)benzeneboronicacid98%
  • 3,5-DI(TRIFLUOROMETHYL)PHENYLBORONIC ACID
  • 3,5-Bis(trifluoroMethyl)benzeneboronic
  • 3,5-Di(trifluoromethyl)benzeneboronic acid
  • 3,5-Bis(trifluoroMethyl)benzeneboronic acid (contains varying aMounts of anhydride)
  • 3,5--TrifluoroMethyl benzene boronic acid
  • AKOS BRN-0072
  • 3,5-BIS(TRIFLUOROMETHYL)BENZENEBORONIC ACID
  • 3,5-BIS(TRIFLUOROMETHYL)PHENYLBOROIC ACID
  • 3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC ACID
  • 3,5-bis-(Trifluoromethyl)benzenboric acid
  • 3,5-bis-(Trifluoromethyl)phenylboric acid
  • 3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC
  • Boronic acid, B-[3,5-bis(trifluoromethyl)phenyl]-
  • 3,5-Bis(trifluoromethyl)phenylboronic acid 98%
  • 3,5-Bis(trifluoromethyl)phenylboronic acid - [B1800]
  • 73852-19-4
  • C8H5O2BF6
  • CF32C6H3BOH2
  • C8H5BF6O2
  • Organometallic Reagents
  • Boronic Acids
  • B (Classes of Boron Compounds)
  • BORONIC ACID
  • Boronic Acids and Derivatives
  • Aryl
  • Substituted Boronic Acids
  • blocks
  • BoronicAcids
  • FluoroCompounds
  • Boric Acid
  • Boronic Acid series
  • Fluorides
  • Fluorin-contained phenyl boronic acid series
  • Boronic Acids
  • Boronic Acids and Derivatives
  • Boronic Acid
  • B (Classes of Boron Compounds)
  • Boronic Acids
  • Aryl
  • Organoborons
  • Trifluoromethyl
  • Boronate Ester
  • Potassium Trifluoroborate