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3-Acetamidophenylboronic acid

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:3-Acetylaminophenyl boronic acid
CAS:78887-39-5
Purity:97% (Min,HPLC) Package:1G;1KG;100KG
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Products Intro: CAS:78887-39-5
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
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Products Intro: Product Name:3-Acetamidophenylboronic acid
CAS:78887-39-5
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Products Intro: Product Name:(3-ACETAMIDOPHENYL)BORONIC ACID
CAS:78887-39-5
Purity:95%+ Package:5g;50g;100g;250g;500g;1kg;5kg
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Products Intro: Product Name:3-Acetamidophenylboronic acid
CAS:78887-39-5
Purity:0.98 Package:1kg,2kg,5kg,10kg,25kg

3-Acetamidophenylboronic acid manufacturers

3-Acetamidophenylboronic acid Basic information
Product Name:3-Acetamidophenylboronic acid
Synonyms:3-(Acetylamino)benzeneboronic acid;RARECHEM AH PB 0113;3-Acetamidophenylboronic acid ,98%;3-Acetamidophenylboronic acid,97%;3-AcetaMidophenylboronic Acid (contains varying aMounts of Anhydride);3-Acetaminophenylboronic acid;Boronicacid, B-[3-(acetylaMino)phenyl]-;3 - N-acetyl-boric acid
CAS:78887-39-5
MF:C8H10BNO3
MW:178.98
EINECS:
Product Categories:Amino;Aryl;Organoborons;Boronic acids;Boronic Acid;Amines;blocks;BoronicAcids
Mol File:78887-39-5.mol
3-Acetamidophenylboronic acid Structure
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
ACROS English
SigmaAldrich English
ALFA English
3-Acetamidophenylboronic acid Usage And Synthesis
Chemical PropertiesOff-white to pale brown powder
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
Usessuzuki reaction
3-Acetamidophenylboronic acid Preparation Products And Raw materials
Preparation ProductsPotassium 3-acetamidophenyltrifluoroborate
Tag:3-Acetamidophenylboronic acid(78887-39-5) Related Product Information
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