4-Ethoxyphenylboronic acid
- Product Name
- 4-Ethoxyphenylboronic acid
- CAS No.
- 22237-13-4
- Chemical Name
- 4-Ethoxyphenylboronic acid
- Synonyms
- AKOS BRN-0070;4-Boronophenetole;RARECHEM AH PB 0138;4-Ethoxyphenylboroni;4-Etoxyphenylboronic acid;P-ETHOXYPHENYLBORONIC ACID;4-ETHOXYPHENYLBORONIC ACID;(4-ethoxyphenyl)boronicaci;4-ETHOXYBENZENEBORONIC ACID;4-Ethoxybenzeneboronicacid,96%
- CBNumber
- CB1724741
- Molecular Formula
- C8H11BO3
- Formula Weight
- 165.98
- MOL File
- 22237-13-4.mol
4-Ethoxyphenylboronic acid Property
- Melting point:
- 121-128 °C(lit.)
- Boiling point:
- 317.6±44.0 °C(Predicted)
- Density
- 1.13±0.1 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- pka
- 8.98±0.10(Predicted)
- form
- solid
- color
- White to Light yellow
- BRN
- 3530408
- InChI
- InChI=1S/C8H11BO3/c1-2-12-8-5-3-7(4-6-8)9(10)11/h3-6,10-11H,2H2,1H3
- InChIKey
- WRQNDLDUNQMTCL-UHFFFAOYSA-N
- SMILES
- B(C1=CC=C(OCC)C=C1)(O)O
- CAS DataBase Reference
- 22237-13-4(CAS DataBase Reference)
Safety
- Hazard Codes
- Xn,Xi
- Risk Statements
- 36/37/38-22
- Safety Statements
- 37/39-26-36
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29163990
- Storage Class
- 11 - Combustible Solids
- Hazard Classifications
- Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
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.
N-Bromosuccinimide Price
- Product number
- 455539
- Product name
- 4-Ethoxyphenylboronic acid
- Packaging
- 1g
- Price
- $32.4
- Updated
- 2023/01/07
- Product number
- 455539
- Product name
- 4-Ethoxyphenylboronic acid
- Packaging
- 10g
- Price
- $106
- Updated
- 2023/01/07
- Product number
- E0725
- Product name
- 4-Ethoxyphenylboronic Acid (contains varying amounts of Anhydride)
- Packaging
- 1g
- Price
- $20
- Updated
- 2025/07/31
- Product number
- E0725
- Product name
- 4-Ethoxyphenylboronic Acid (contains varying amounts of Anhydride)
- Packaging
- 5g
- Price
- $59
- Updated
- 2025/07/31
- Product number
- E892828
- Product name
- 4-Ethoxyphenylboronic acid
- Packaging
- 2.5g
- Price
- $65
- Updated
- 2021/12/16
4-Ethoxyphenylboronic acid Chemical Properties,Usage,Production
Chemical Properties
White crystalline powder
Uses
4-Methoxybenzeneboronic acid is used for suzuki reaction.
Application
Reactant involved in Suzuki cross coupling reactions
Reactant involved in the synthesis of biologically active molecules including:
Novel modulators of survival motor neuron protein for treatment of spinal muscular atrophy
Amino-trimethoxyphenyl-aryl thiazoles for use as microtubule inhibitors and antitumor agents
Bicyclic hydroxyphenyl methanone derivatives for use as hydroxysteroid dehydrogenase inhibitors
Dual immunosuppressive and anti-inflammatory agents
Antiproliferatives via Suzuki cross-coupling / amination reactions
Synthesis
A hexane solution of butyllithium (30 mL, 1.58 M, 47 mmol) was added dropwise to a THF solution (50 mL) of 2-bromo-??,??-trifluorotoluene (9.79 g, 43.5 mmol) at -78?? C. The aryllithium was then transferred to a THF solution of B(OEt)3 (30 mL, 176 mmol) by cannulae. After stirring at this temperature for 3 hours, the resulting aryl lithium was transferred via cannula to a THF solution (100 mL) of triethyl borate (B(OEt)3, 30 mL, 176 mmol) (aryl lithium may be unstable at higher temperatures. We recommend making the transfer as soon as possible). Warm the reaction mixture to room temperature and stir overnight. Hydrochloric acid (2M, 80 mL) was added and the mixture was extracted with ethyl acetate. The combined organic layers were dried with anhydrous sodium sulfate and then evaporated under vacuum. The desired boric acid was dissolved in hot toluene and separated from the toluene-insoluble residue. The combined toluene solutions were evaporated and the remaining solid was recrystallized from toluene to give 4-ethoxyphenylboronic acid in 6.02 g, 73% yield. Yield 16%.
4-Ethoxyphenylboronic acid Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 4-Ethoxyphenylboronic acid manufacturers
- Product
- 4-ETHOXYPHENYLBORONIC ACID 22237-13-4
- Price
- US $15.00-10.00/KG
- Min. Order
- 1KG
- Purity
- 99%+ HPLC
- Supply Ability
- Monthly supply of 1 ton
- Release date
- 2021-07-10
- Product
- 4-ETHOXYPHENYLBORONIC ACID 22237-13-4
- Price
- US $15.00-10.00/KG
- Min. Order
- 1KG
- Purity
- 99%+ HPLC
- Supply Ability
- Monthly supply of 1 ton
- Release date
- 2021-07-09
- Product
- 4-ETHOXYPHENYLBORONIC ACID 22237-13-4
- Price
- US $1.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 1000kg
- Release date
- 2018-12-17