ChemicalBook > CAS DataBase List > 3,5-Dimethoxyphenylboronic acid

3,5-Dimethoxyphenylboronic acid

Product Name
3,5-Dimethoxyphenylboronic acid
CAS No.
192182-54-0
Chemical Name
3,5-Dimethoxyphenylboronic acid
Synonyms
3,5-DimethoxyphenyL;3,5-DIMETHOXYBENZENEBORONIC ACID;AKOS BRN-0893;5-DiMethoxyphenylboronic acid;3,5-DIMETHOXYPHENYLBORONIC ACID;B-(3,5-dimethoxyphenyl)boronic acid;3,5-DIMETHOXYPHENYLBORONIC ACID 99%;3,5-Dimethoxyphenylboronic acid ,98%;3,5-Dimethoxyphenylboronic acid >=95%;Boronic acid, B-(3,5-dimethoxyphenyl)-
CBNumber
CB6716893
Molecular Formula
C8H11BO4
Formula Weight
181.98
MOL File
192182-54-0.mol
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3,5-Dimethoxyphenylboronic acid Property

Melting point:
202-207 °C
Boiling point:
371.6±52.0 °C(Predicted)
Density 
1.19±0.1 g/cm3(Predicted)
Flash point:
81℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Soluble in methanol.
pka
7.67±0.10(Predicted)
form 
powder to crystal
color 
White to Light yellow to Light orange
CAS DataBase Reference
192182-54-0(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
Hazard Note 
Irritant/Keep Cold
HazardClass 
IRRITANT, KEEP COLD
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.

P271Use only outdoors or in a well-ventilated area.

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
715271
Product name
3,5-Dimethoxyphenylboronic acid
Purity
≥95%
Packaging
1g
Price
$16.45
Updated
2025/07/31
Sigma-Aldrich
Product number
715271
Product name
3,5-Dimethoxyphenylboronic acid
Purity
≥95%
Packaging
5g
Price
$121
Updated
2025/07/31
TCI Chemical
Product number
D3513
Product name
3,5-Dimethoxyphenylboronic Acid (contains varying amounts of Anhydride)
Packaging
1g
Price
$33
Updated
2025/07/31
TCI Chemical
Product number
D3513
Product name
3,5-Dimethoxyphenylboronic Acid (contains varying amounts of Anhydride)
Packaging
5g
Price
$91
Updated
2025/07/31
TCI Chemical
Product number
D3513
Product name
3,5-Dimethoxyphenylboronic Acid (contains varying amounts of Anhydride)
Packaging
25g
Price
$301
Updated
2025/07/31
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3,5-Dimethoxyphenylboronic acid Chemical Properties,Usage,Production

Chemical Properties

Gray to white solid

Uses

3,5-Dimethoxyphenylboronic acid is a useful reagent for palladium-catalyst and Suzuki-Miyaura cross coupling reactions.

Uses

Reactant for:

  • Palladium-catalyzed coupling reactions
  • Preparation of benzopyranone derivatives as positive GABAA receptor modulators
  • Preparation of aryl alkenes via three-component coupling catalyzed by palladium
  • Suzuki-Miyaura coupling
  • Rhodium catalyzed cyanation with N-cyano-N-phenyl-p-methylbenzenesulfonamide
  • Preparation of bisphosphonate inhibitors of human farnesyl pyrophosphate synthase

Uses

suzuki reaction

Synthesis

5419-55-6

20469-65-2

192182-54-0

1. Synthesis of 3,5-dimethoxyphenylboronic acid: After cooling the flame-dried reaction vessel under argon protection, 3,5-dimethoxybromobenzene (3 g, 13.82 mmol) and anhydrous tetrahydrofuran (36 ml) were added. The mixture was stirred until a clarified solution was formed. Subsequently, the reaction mixture was cooled to -78 °C and maintained at this temperature for 15 minutes. n-Butyllithium (10.92 ml, 2.1 M hexane solution) was slowly added and the reaction mixture continued to be stirred at -78 °C for 30 minutes. Then, triisopropyl borate (5.2 g, 27.64 mmol) was added dropwise and the reaction was continuously stirred at -78°C for 2 hours. After completion of the reaction, it was slowly warmed up to room temperature and acidified with 2 M sulfuric acid solution to pH 2. The reaction mixture was extracted with ethyl acetate, the organic phases were combined, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was purified by recrystallization from petroleum ether to give 3,5-dimethoxyphenylboronic acid in 92% yield.

References

[1] Patent: WO2008/118802, 2008, A1. Location in patent: Page/Page column 25-26

3,5-Dimethoxyphenylboronic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 3,5-Dimethoxyphenylboronic acid manufacturers

Zhuozhou Wenxi import and Export Co., Ltd
Product
3,5-Dimethoxyphenylboronic acid 192182-54-0
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
Zhuozhou Wenxi import and Export Co., Ltd
Product
3,5-Dimethoxyphenylboronic acid 192182-54-0
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
Hebei shuoxi biotechnology co. LTD
Product
(3,5-dimethoxyphenyl)boronic acid 192182-54-0
Price
US $80.00/g
Min. Order
10g
Purity
99.8%
Supply Ability
10tons
Release date
2020-04-10

192182-54-0, 3,5-Dimethoxyphenylboronic acidRelated Search:


  • 3,5-DimethoxyphenyL
  • 3,5-Dimethoxyphenylboronic Acid (contains varying amounts of Anhydride)
  • 3,5-Dimethoxyphenylboronic acid, (contains various amounts of anhydride)
  • 3,5-Dimethoxyphenylboronic acid ,98%
  • 3,5-Dimethoxyphenylboronic Acid, (Contains Various Amounts Of Anhydr
  • B-(3,5-dimethoxyphenyl)boronic acid
  • 5-DiMethoxyphenylboronic acid
  • 3,5-DIMETHOXYPHENYLBORONIC ACID
  • 3,5-DIMETHOXYBENZENEBORONIC ACID
  • AKOS BRN-0893
  • Boronic acid, B-(3,5-dimethoxyphenyl)-
  • 3,5-Dimethoxyphenylboronic acid >=95%
  • 3,5-DIMETHOXYPHENYLBORONIC ACID 99%
  • 192182-54-0
  • C8H11O4B
  • B (Classes of Boron Compounds)
  • Boronic Acids
  • blocks
  • BoronicAcids
  • Heterocyclic Compounds
  • Boronic Acid