Methyl 4-boronobenz...

Methyl 4-boronobenzoate

Methyl 4-boronobenzoate

Min.Order / FOB Price:Get Latest Price

1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 98.00%
  • Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

99768-12-4 Methyl 4-boronobenzoate 4-METHOXYCATBONYLPHENYLBORONICACID

Quick Details

  • Appearance:white crystalline powder
  • Application:For Pharmaceutical industry
  • PackAge:as per buyers
  • ProductionCapacity:1|Metric Ton|Month
  • Storage:Room temperature
  • Transportation:Shipment as non- dangerous chemicals by sea or air

Superiority:

Methyl 4-boronobenzoate Basic information
Product Name: Methyl 4-boronobenzoate
Synonyms: RARECHEM AH PB 0115;P-(METHOXYCARBONYL)PHENYLBORONIC ACID;METHYL 4-BORONOBENZOATE;AKOS BRN-0122;4-METHOXYCARBONYLBENZENEBORONIC ACID;4-METHOXYCARBONYLPHENYLBORONIC ACID;4-CARBOMETHOXYPHENYLBORONIC ACID;4-METHOXYCATBONYLPHENYLBORONICACID
CAS: 99768-12-4
MF: C8H9BO4
MW: 179.97
EINECS:  
Product Categories: blocks;BoronicAcids;Carboxes;Boronic Acid series;Acids and Derivatives;Boron, Nitrile, Thio,& TM-Cpds;Boronic acids;Aryl;Boronic acid;Organoborons;B (Classes of Boron Compounds);CHIRAL CHEMICALS;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boronate Ester;Potassium Trifluoroborate
Mol File: 99768-12-4.mol
Methyl 4-boronobenzoate Structure

 

Details:

Methyl 4-boronobenzoate Chemical Properties
mp  197-200 °C(lit.)
storage temp.  0-6°C
CAS DataBase Reference 99768-12-4(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  37/39-26
WGK Germany  3
HazardClass  IRRITANT
 
Methyl 4-boronobenzoate Usage And Synthesis
Chemical Properties White to light yellow crystal powde
Usage Reagent used for• ;Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence1 • ;Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2 • ;One-pot ipso-nitration of arylboronic acids3 • ;Copper-catalyzed nitration4 • ;Cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling5 • ;Reagent used in Preparation of• ;Biaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid6† • ;Chromenones and their
Usage suzuki reaction

 

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