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

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
Molecular Weight:
257.93
MDL Number:
MFCD00051850
MOL File:
73852-19-4.mol
Last updated:2026-01-13 11:23:07
Product description Number Pack Size Price
3,5-Bis(trifluoromethyl)phenylboronic acid ≥95% 471070 5g $78.27
3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride) B1886 1g $21
3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride) B1886 5g $58
3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride) B1886 25g $172
3,5-Bis(trifluoromethyl)phenylboronic acid B412868 5g $55
More product size

3,5-Bis(trifluoromethyl)benzeneboronic acid Properties

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
pka 6.57±0.10(Predicted)
form Crystals or Powder
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)
UNSPSC Code 12352103
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  37/39-26
WGK Germany  3
TSCA  No
HazardClass  IRRITANT
HS Code  29163990
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

3,5-Bis(trifluoromethyl)benzeneboronic acid price More Price(48)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 471070 3,5-Bis(trifluoromethyl)phenylboronic acid ≥95% 73852-19-4 5g $78.27 2025-07-31 Buy
TCI Chemical B1886 3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride) 73852-19-4 1g $21 2025-07-31 Buy
TCI Chemical B1886 3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride) 73852-19-4 5g $58 2025-07-31 Buy
TCI Chemical B1886 3,5-Bis(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride) 73852-19-4 25g $172 2025-07-31 Buy
TRC B412868 3,5-Bis(trifluoromethyl)phenylboronic acid 73852-19-4 5g $55 2021-12-16 Buy
Product number Packaging Price Buy
471070 5g $78.27 Buy
B1886 1g $21 Buy
B1886 5g $58 Buy
B1886 25g $172 Buy
B412868 5g $55 Buy

3,5-Bis(trifluoromethyl)benzeneboronic acid Chemical Properties,Uses,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

Trimethyl borate

121-43-7

3,5-Bis(trifluoromethyl)bromobenzene

328-70-1

Water

7732-18-5

3,5-Bis(trifluoromethyl)benzeneboronic acid

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

Global( 352)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055 Sibel@chuanghaibio.com China 8753 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718; +8613336195806 sales@capot.com China 29735 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-2158073036 info@dakenam.com China 13620 58
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29833 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
Wuhan Chemwish Technology Co., Ltd
027-67849912 sales@chemwish.com CHINA 10821 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49977 58
Richest Group Ltd
18017061086 oled@richest-group.com CHINA 5600 58
Neostar United (Changzhou) Industrial Co., Ltd.
+86-0519-85551759 +8613506123987 marketing1@neostarunited.com China 8830 58

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

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3,5-Bis(trifluoromethyl)benzeneboronic acid pictures 2026-01-05 3,5-Bis(trifluoromethyl)benzeneboronic acid
73852-19-4
US $1.00 / KG 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
3,5-Bis(trifluoromethyl)benzeneboronic acid pictures 2019-07-06 3,5-Bis(trifluoromethyl)benzeneboronic acid
73852-19-4
US $1.00 / KG 1KG 97%-99% 100kg Career Henan Chemical Co
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