ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid 4-Carbamoylphenylboronic acid

4-Carbamoylphenylboronic acid

4-Carbamoylphenylboronic acid Basic information
Product Name:4-Carbamoylphenylboronic acid
Synonyms:BENZAMIDE-4-BORONIC ACID;4-CARBOXAMIDEPHENYLBORONIC ACID;4-CARBAMOYLPHENYLBORONIC ACID;(4-AMINOCARBONYL)BENZENEBORONIC ACID;4-AMINOCARBONYLPHENYLBORONIC ACID;P-(AMINOCARBONYL)PHENYLBORONIC ACID;4-(Aminocarbonyl)Phenylboronic;4-Carbamoylbenzeneboronic acid
CAS:123088-59-5
MF:C7H8BNO3
MW:164.95
EINECS:
Product Categories:Boronate Ester;Potassium Trifluoroborate;Amide;Aryl;Organoborons;Boronic acid;blocks;BoronicAcids;Carboxes;Boronic acids
Mol File:123088-59-5.mol
4-Carbamoylphenylboronic acid Structure
4-Carbamoylphenylboronic acid Chemical Properties
Melting point 242-252°C
Boiling point 414.3±47.0 °C(Predicted)
density 1.32±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility soluble in Methanol
pka7.87±0.10(Predicted)
form powder or crystals
color white to off-white
InChIKeyGNRHNKBJNUVWFZ-UHFFFAOYSA-N
CAS DataBase Reference123088-59-5(CAS DataBase Reference)
Safety Information
Hazard Codes C,Xi,Xn
Risk Statements 36/37/38-22-20/21/22
Safety Statements 26-36/37/39-36-24/25
WGK Germany 3
Hazard Note Corrosive
TSCA No
HazardClass IRRITANT
HS Code 29310095
MSDS Information
4-Carbamoylphenylboronic acid Usage And Synthesis
Chemical PropertiesWhite to brown solid
UsesReactant involved in:
  • Suzuki-Miyaura, Sonogashira and Buchwald-Hartwig cross-coupling reactions for the synthesis of substituted pyrene derivatives
  • Suzuki-Miyaura reactions for the synthesis of aryl-substituted oxabenzindoles and methanobenzindoles or 2-aminoimidazole triazoles
  • Three-component coupling with triflates and alkenes

Reactant involved in synthesis of biologically active molecules including:
  • Hybrid peptidomimetic molecules as STAT3 protein inhibitors
  • Vasopressin V1B receptor antagonists for use as antidepressants oand anxiolytics
  • (Thienopyridine)caboxamides as CHK1 inhibitors
Usessuzuki reaction
4-Carbamoylphenylboronic acid Preparation Products And Raw materials
Raw materials4-Carboxyphenylboronic acid
4-Aminophenylboronic acid 4-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID 4-(N,O-DIMETHYLHYDROXYLAMINOCARBONYL)PHENYLBORONIC ACID 4-(CYCLOPENTYLAMINOCARBONYL)PHENYLBORONIC ACID 4-(N-METHYLAMINOCARBONYL)PHENYLBORONIC ACID 4-(BUTYLAMINOCARBONYL)PHENYLBORONIC ACID Phenylboronic acid 4-(MORPHOLINE-4-CARBONYL)PHENYLBORONIC ACID 4-Carbamoylphenylboronic acid 4-(TERT-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID 4-(N-BENZYLAMINOCARBONYL)PHENYLBORONIC ACID 4-(CYCLOHEXYLAMINOCARBONYL)PHENYLBORONIC ACID 2-(Trifluoromethoxy)aniline 4-(Cyclopropylaminocarbonyl)phenylboronic acid p-Aminobenzamide 4-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID 4-(N-Isopropylaminocarbonyl)phenylboronic acid 4-(ISOBUTYLAMINOCARBONYL)PHENYLBORONIC ACID
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