Basic information Safety Supplier Related

3,5-Dimethyl-4-methoxyphenylboronic acid

Basic information Safety Supplier Related

3,5-Dimethyl-4-methoxyphenylboronic acid Basic information

Product Name:
3,5-Dimethyl-4-methoxyphenylboronic acid
Synonyms:
  • CHEMBRDG-BB 4003302
  • 4-METHOXY-3,5-DIMETHYLBENZENEBORONIC ACID
  • 3,5-DIMETHYL-4-METHOXYBENZENEBORONIC ACID
  • 3,5-DIMETHYL-4-METHOXYPHENYLBORONIC ACID
  • AKOS BRN-0232
  • 3,5-Dimethyl-4-methoxybenzeneboronic acid~4-Methoxy-3,5-dimethylphenylboronic acid
  • 3,5-DIMENTHYL-4-METHOXYPHENYLBORONIC ACID
  • 3,5-Dimethyl-4-Methoxyphenylbo
CAS:
301699-39-8
MF:
C9H13BO3
MW:
180.01
Product Categories:
  • Organoborons
  • Aryl Boronic Acids
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Organometallic Reagents
  • Trisubstituted Aryl Boronic Acids
  • blocks
  • BoronicAcids
  • Boronic acids
  • Heterocyclic Compounds
  • Aryl
  • Boronic Acids
  • Boronic Acids and Derivatives
Mol File:
301699-39-8.mol
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3,5-Dimethyl-4-methoxyphenylboronic acid Chemical Properties

Melting point:
235-242 °C (lit.)
Boiling point:
335.8±52.0 °C(Predicted)
Density 
1.11±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
soluble in Methanol
form 
powder to crystal
pka
9.08±0.11(Predicted)
color 
White to Almost white
BRN 
8205051
CAS DataBase Reference
301699-39-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29319090

MSDS

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3,5-Dimethyl-4-methoxyphenylboronic acid Usage And Synthesis

Uses

Reactant for:• ;Preparation of biologically and pharmacologically active molecules1,2• ;Suzuki and Stille cross-coupling reaction3• ;Mizoroki-Heck arylation4• ;Baeyer-Villiger oxidation5• ;Rhodium-catalyzed asymmetric conjugate addition reactions6

Uses

suzuki reaction

Uses

Reactant for:

  • Preparation of biologically and pharmacologically active molecules
  • Suzuki and Stille cross-coupling reaction
  • Mizoroki-Heck arylation
  • Baeyer-Villiger oxidation
  • Rhodium-catalyzed asymmetric conjugate addition reactions

3,5-Dimethyl-4-methoxyphenylboronic acidSupplier

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