3-Aminocarbonylphen...

3-Aminocarbonylphenylboronic acid-

3-Aminocarbonylphenylboronic acid-

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1 Gram

Negotiable

  • Min.Order :1 Gram
  • Purity: 98%
  • Payment Terms : L/C,D/A,D/P,T/T,

Keywords

BENZAMIDE-3-BORONIC ACID 3-CARBAMOYLPHENYLBORONIC ACID;3-CARBAMOYLPHENYLBORONIC ACID, 3-BORONOBENZAMIDE;3-CARBOXAMIDEPHENYLBORONIC ACID;3-(AMINOCARBONYL)BENZENEBORONIC ACID 3-AMINOCARBONYLPHENYLBORONIC ACID;3-AMINOCARBONYLPENYLBORONIC ACID;3-Aminocarbonyiphenylboronic acid

Quick Details

  • Appearance:White to brown solid
  • Application:351422-73-6
  • PackAge:woven bags, drum, kraft paper bag or customer's request
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:N/A
  • Transportation:--

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1.Noble Metal Catalysts (Pt.Pd...)

2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)

3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

4.Customs Synthesis

 

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Details:

3-Aminocarbonylphenylboronic acid Basic information

Product Name: 3-Aminocarbonylphenylboronic acid
Synonyms: BENZAMIDE-3-BORONIC ACID;3-CARBAMOYLPHENYLBORONIC ACID;3-CARBAMOYLPHENYLBORONIC ACID, 3-BORONOBENZAMIDE;3-CARBOXAMIDEPHENYLBORONIC ACID;3-(AMINOCARBONYL)BENZENEBORONIC ACID;3-AMINOCARBONYLPHENYLBORONIC ACID;3-AMINOCARBONYLPENYLBORONIC ACID;3-Aminocarbonyiphenylboronic acid
CAS: 351422-73-6
MF: C7H8BNO3
MW: 164.95
EINECS:  
Product Categories: blocks;BoronicAcids;Carboxes;Boronic acids;Heterocyclic Compounds;Amide;Aryl;Organoborons;Boronic acid;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boronate Ester;Potassium Trifluoroborate
Mol File: 351422-73-6.mol
3-Aminocarbonylphenylboronic acid Structure
 
3-Aminocarbonylphenylboronic acid Chemical Properties
mp  232-235°C
storage temp.  Keep Cold
CAS DataBase Reference 351422-73-6(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xi,Xn
Risk Statements  22-36/37/38-20/21/22
Safety Statements  26-36
Hazard Note  Corrosive
HazardClass  IRRITANT
HS Code  29310095
 
 
3-Aminocarbonylphenylboronic acid Usage And Synthesis
Chemical Properties White to brown solid
Usage Reactant involved in the synthesis of a variety of inhibitors including:• ;Orally active phosphodiesterase 10A inhibitors1• ;Pyrimidine derivatives as TpI2 kinase inhibitors2• ;Peptidomimetic inhibitors of STAT3 protein3Reactant involved in:• ;Oxidative cross-coupling with mercaptoacetylenes4• ;Trifluoromethylation via a Collidine trifluoromethylating agent5• ;Suzuki cross-coupling reactions6
Usage suzuki reaction

 

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