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4-BUTOXY-3-FLUOROPHENYLBORONIC ACID

Product Name
4-BUTOXY-3-FLUOROPHENYLBORONIC ACID
CAS No.
156487-13-7
Chemical Name
4-BUTOXY-3-FLUOROPHENYLBORONIC ACID
Synonyms
Boronic acid, B-(4-butoxy-3-fluorophenyl)-
CBNumber
CB3498525
Molecular Formula
C10H14BFO3
Formula Weight
212.03
MOL File
156487-13-7.mol
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4-BUTOXY-3-FLUOROPHENYLBORONIC ACID Property

Melting point:
91-96 °C(lit.)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
Appearance
White to off-white Solid
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Safety

WGK Germany 
3
HS Code 
2931900090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B695085
Product name
4-Butoxy-3-fluorophenylboronicAcid
Packaging
50mg
Price
$55
Updated
2021/12/16
AK Scientific
Product number
X1333
Product name
4-Butoxy-3-fluorophenylboronicacid
Packaging
1g
Price
$117
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
BOR0000648
Product name
4-BUTOXY-3-FLUOROPHENYLBORONIC ACID
Purity
95.00%
Packaging
1G
Price
$210
Updated
2021/12/16
AK Scientific
Product number
X1333
Product name
4-Butoxy-3-fluorophenylboronicacid
Packaging
5g
Price
$317
Updated
2021/12/16
Ambeed
Product number
A622538
Product name
(4-Butoxy-3-fluorophenyl)boronicacid
Purity
95%
Packaging
250mg
Price
$13
Updated
2021/12/16
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4-BUTOXY-3-FLUOROPHENYLBORONIC ACID Chemical Properties,Usage,Production

Synthesis

121-43-7

54509-63-6

156487-13-7

4-Butoxy-3-fluorophenylboronic acid (T-9) was synthesized as follows: 4-bromo-1-butoxy-2-fluorobenzene (T-8) (97.5 g) prepared in the previous step was dissolved in dry tetrahydrofuran (THF) (500 ml) and the solution was cooled to -70 °C. Under nitrogen protection, n-butyllithium (n-BuLi) (241 ml) was slowly added dropwise with continuous stirring for 2 h at a maintained temperature of -70°C. Subsequently, a dry THF solution of trimethyl borate (62.4 g) was slowly added dropwise to the reaction system at the same temperature. The reaction mixture was gradually warmed to room temperature and stirring was continued for 16 hours. After completion of the reaction, 2N hydrochloric acid (HCl) (200 ml) was added to the reaction mixture for acidification. The mixture was extracted with toluene and after separating the organic layer, it was washed sequentially with water and saturated saline and finally dried with anhydrous magnesium sulfate. The organic phase was concentrated under reduced pressure to give a light brown solid product. Purification by recrystallization (solvent ratio: heptane/toluene=4:1, v/v) gave the target compound 4-butoxy-3-fluorophenylboronic acid (T-9) as a colorless powder (54.8 g) in 66% yield.

References

[1] Patent: EP2399896, 2011, A1. Location in patent: Page/Page column 38

4-BUTOXY-3-FLUOROPHENYLBORONIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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4-BUTOXY-3-FLUOROPHENYLBORONIC ACID Suppliers

SIGMA-RBI
Tel
--
Fax
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Country
Switzerland
ProdList
6896
Advantage
91
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View Lastest Price from 4-BUTOXY-3-FLUOROPHENYLBORONIC ACID manufacturers

Career Henan Chemical Co
Product
4-BUTOXY-3-FLUOROPHENYLBORONIC ACID 156487-13-7
Price
US $1.00/KG
Min. Order
1KG
Purity
99.0%
Supply Ability
100kg
Release date
2020-01-14