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4-Methoxycarbonylphenylboronic acid

CAS NO.99768-12-4

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  • Min.Order: 100 Kilogram
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Product Details

Keywords

  • RARECHEM AH PB 0251
  • 99768-12-4
  • C8H9BO4

Quick Details

  • ProName: 4-Methoxycarbonylphenylboronic acid
  • CasNo: 99768-12-4
  • Molecular Formula: C8H9BO4
  • Appearance: powder
  • Application: 99768-12-4
  • DeliveryTime: Within 3-7 days
  • PackAge: Depended
  • Port: China Main Port
  • ProductionCapacity: 300 Kilogram/Month
  • Purity: 99%
  • Storage: Refrigerator
  • Transportation: by air or by sea
  • LimitNum: 100 Kilogram
  • Valid Period: 6 month
  • Application: Multipurpose intermediate
  • Application: ISO/9001 Certificate

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
 
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
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
 
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
 
Methyl 4-boronobenzoate Preparation Products And Raw materials
Raw materials Methanol-->Tetrahydrofuran-->Nitrogen-->Potassium permanganate-->Magnesium-->Trimethyl borate-->4-Bromotoluene
 
 

 

 

 

 

 

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