3-Acetamidophenylboronic acid

3-Acetamidophenylboronic acid
  • CAS No.:78887-39-5
Other grades of this product :
3-Acetamidophenylboronic acid Basic information
Product Name:3-Acetamidophenylboronic acid
Synonyms:Boronicacid, B-[3-(acetylaMino)phenyl]-;3 - N-acetyl-boric acid;3-(Acetylamino)benzeneboronic acid, 3'-Boronoacetanilide;TIMTEC-BB SBB000203;3-ACETAMIDOPHENYLBORONIC ACID;3-ACETAMIDOBENZENEBORONIC ACID;3-ACETYLAMINOPHENYLBORONIC ACID;M-ACETAMIDOPHENYLBORONIC ACID
CAS:78887-39-5
MF:C8H10BNO3
MW:178.98
EINECS:
Product Categories:Amino;Aryl;Amines;Boronic acids;Boronic Acid;Organoborons;blocks;BoronicAcids
Mol File:78887-39-5.mol
3-Acetamidophenylboronic acid Chemical Properties
Melting point 135 °C (lit.)
density 1.23±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
pka8.04±0.10(Predicted)
form powder
color Light orange to Yellow to Green
BRN 3278316
CAS DataBase Reference78887-39-5(CAS DataBase Reference)
EPA Substance Registry SystemBoronic acid, B-[3-(acetylamino)phenyl]- (78887-39-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36-26-37
WGK Germany 3
3-10
HazardClass IRRITANT
HS Code 29310095
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
3-Acetamidophenylboronic acid Usage And Synthesis
Chemical PropertiesOff-white to pale brown powder
Usessuzuki reaction
UsesReactant involved in:
  • Suzuki-Miyaura coupling reactions
  • Trifluoromethylation
Reactant involved in the synthesis of a variety of inhibitors including:
  • NR2B subtype of NMDA receptor antagonists for antidepressant activity
  • Biphenylylmethylimidazole derivatives for use as 17,20-lyase inhibitors
  • (Indolyl)-3,5-substituted benzene analogs with antimitotic and antitumor activity
  • Substituted pyrrolidines and tetrahydrofurans as AMPA receptor positive modulators
3-Acetamidophenylboronic acid Preparation Products And Raw materials

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