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3-Acetamidophenylboronic acid

Basic information Safety Supplier Related

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
Product Categories:
  • Amino
  • Aryl
  • Amines
  • Boronic acids
  • Boronic Acid
  • Organoborons
  • blocks
  • BoronicAcids
Mol File:
78887-39-5.mol
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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
pka
8.04±0.10(Predicted)
form 
powder
color 
Light orange to Yellow to Green
BRN 
3278316
CAS DataBase Reference
78887-39-5(CAS DataBase Reference)
EPA Substance Registry System
Boronic acid, B-[3-(acetylamino)phenyl]- (78887-39-5)
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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

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3-Acetamidophenylboronic acid Usage And Synthesis

Chemical Properties

Off-white to pale brown powder

Uses

suzuki reaction

Uses

Reactant 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

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