4-Methoxyphenylboro...

4-Methoxyphenylboronic acid 5720-07-0

4-Methoxyphenylboronic acid 5720-07-0

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1 Metric Ton

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  • Purity: 99
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Keywords

5720-07-0 4-Methoxyphenylboronic acid 4-Methoxyphenylboronic acid

Quick Details

  • Appearance:Colorless Liquid
  • Application:FOR ORGANIC SYNTHESIS USE
  • PackAge:According customer request
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:In Room Temperature
  • Transportation:AS PER MSDS

Superiority:


Product Name: 4-Methoxyphenylboronic acid
Synonyms: (4-methoxyphenyl)-boronicaci;p-methoxy-benzeneboronicaci;p-methoxyphenyl-boronicaci;RARECHEM AH PB 0191;P-METHOXYPHENYLBORONIC ACID;p-methoxybenzeneboronic acid;p-Anisylboronic acid;TIMTEC-BB SBB004055
CAS: 5720-07-0
MF: C7H9BO3
MW: 151.96
EINECS: 216-845-5
Product Categories: blocks;BoronicAcids;Boronic Acid series;Substituted Boronic Acids;Boronic acids;Heterocyclic Compounds;Boronic Acid;Alkoxy;Aryl;Organoborons;B (Classes of Boron Compounds);organic or inorganic borate;Aromatics;Intermediates;Miscellaneous Reagents;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boron Derivatives;Boronate Ester;Potassium Trifluoroborate
Mol File: 5720-07-0.mol
4-Methoxyphenylboronic acid Structure

Details:

4-Methoxyphenylboronic acid Chemical Properties
mp  204-206 °C(lit.)
storage temp.  Refrigerator (+4°C)
BRN  2936912
CAS DataBase Reference 5720-07-0(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
RTECS  CY8975000
Hazard Note  Irritant
HazardClass  IRRITANT
HS Code  29310095
 
4-Methoxyphenylboronic acid Usage And Synthesis
Chemical Properties white to light beige crystalline powder
Usage Reagent used in the preparation of various biological inhibitors.
Usage Reagent used for• ;Suzuki-Miyaura cross-coupling reactions1 • ;Pd-catalyzed direct arylation2 • ;Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water3 • ;Palladium-catalyzed stereoselective Heck-type reaction4 • ;Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence5 • ;Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides6 • ;Ruthenium catalyzed direct arylation7 • ;Rh-catalyzed asymmetric conjugate addition8 R
Usage 4-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants.
Usage suzuki reaction

 

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