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ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Borate >  Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

Basic information Safety Supplier Related

Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate Basic information

Product Name:
Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
Synonyms:
  • 4-METHOXYCARBONYLPHENYLBORONIC ACID, PINACOL ESTER
  • 4-METHOXYCARBONYLPHENYLBORONIC ACID PINACOLATE
  • 4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)BENZOIC ACID METHYL ESTER
  • 2-(4-CARBOMETHOXYPHENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE
  • 4-carbomethoxyphenylboronic acid pinacol ester
  • METHYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE
  • Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2
  • 4-(Methoxycarbonyl)benzeneboronic acid pinacol ester, 97%
CAS:
171364-80-0
MF:
C14H19BO4
MW:
262.11
Product Categories:
  • Aryl Boronate Esters
  • Boronate Esters
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Organometallic Reagents
  • Heterocyclic Compounds
  • Acids and Derivatives
  • Boron, Nitrile, Thio,& TM-Cpds
  • CHIRAL CHEMICALS
Mol File:
171364-80-0.mol
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Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate Chemical Properties

Melting point:
77-81 °C(lit.)
Boiling point:
355.6±25.0 °C(Predicted)
Density 
1.08±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Crystalline Powder
color 
White
InChI
InChI=1S/C14H19BO4/c1-13(2)14(3,4)19-15(18-13)11-8-6-10(7-9-11)12(16)17-5/h6-9H,1-5H3
InChIKey
REIZEQZILPXYKS-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C(B2OC(C)(C)C(C)(C)O2)C=C1
CAS DataBase Reference
171364-80-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37
WGK Germany 
3
TSCA 
No
HS Code 
29310099

MSDS

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Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate Usage And Synthesis

Uses

Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate was used to prepare 2-aryl-4,4,5,5,-tetramethyl-1,3,2-dioxaborolanes via palladium-catalyzed coupling reactions.

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