4-Aminophthalide

4-Aminophthalide Suppliers list
Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:4-Amino-3H-isobenzofuran-1-one
CAS:59434-19-4
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:4-Aminophthalide
CAS:59434-19-4
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-69969
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Products Intro: Product Name:4-Aminophthalide
CAS:59434-19-4
Purity:98% HPLC Package:1KG;1USD
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Products Intro: Product Name:4-Aminoisobenzofuran-1(3H)-one
CAS:59434-19-4
Purity:0.98 Package:1kg; 25kg; or larger package as required Remarks:pharmaceutical intermediates;Chemical Intermediate
Company Name: Hefei TNJ Chemical Industry Co.,Ltd.
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Products Intro: Product Name:4-Aminophthalide
CAS:59434-19-4

4-Aminophthalide manufacturers

  • 4-Aminophthalide
  • 4-Aminophthalide pictures
  • $1.00
  • 2020-01-10
  • CAS:59434-19-4
  • Min. Order: 1KG
  • Purity: 98% HPLC
  • Supply Ability: 10 tons/month
4-Aminophthalide Basic information
Product Name:4-Aminophthalide
Synonyms:4-Amino-2-benzofuran-1(3H)-one;4-Amino-3H-isobenzofuran-1-one;4-Aminophthalide;4-aMinoisobenzofuran-1(3H)-one;1(3H)-Isobenzofuranone, 4-amino-;Lenalidomide Impurity 99;4-amino-3H-2-benzofuran-1-one
CAS:59434-19-4
MF:C8H7NO2
MW:149.15
EINECS:
Product Categories:Heterocycles;Heterocyclic Compound
Mol File:59434-19-4.mol
4-Aminophthalide Structure
4-Aminophthalide Chemical Properties
Melting point 154-155 °C
Boiling point 411.0±45.0 °C(Predicted)
density 1.376
storage temp. 2-8°C, protect from light
pka2.70±0.20(Predicted)
AppearanceOff-white to light brown Solid
Safety Information
HS Code 2932990090
MSDS Information
4-Aminophthalide Usage And Synthesis
Uses4-Aminophthalide acts as a reagent in the synthesis of butylphthalide derivatives with medical applications.
Synthesis
4-Nitrophthalide

65399-18-0

4-Aminophthalide

59434-19-4

General procedure for the synthesis of 4-aminoisobenzofuran-1(3H)-one from 4-nitroisobenzofuran-1(3H)-one: 4-nitroisobenzofuran-1(3H)-one (1.0 g, 5.58 mmol) and 10% Pd/C (0.1 g) were suspended in ethyl acetate (30 mL). The reaction system was purged with hydrogen (1 atm) and stirred for 3 hours at 25°C. After completion of the reaction, the mixture was filtered to remove the catalyst and the filtrate was concentrated to afford 4-aminoisobenzofuran-1(3H)-one (0.8 g, 96% yield) as an off-white solid. Mass spectrum (ESI) m/z: 150 (M + 1)+. 1H-NMR (400 MHz, CDCl3) δ 3.82 (s, broad peak, 1H), 5.19 (s, 3H), 6.91-6.95 (m, 1H), 7.32-7.36 (m, 2H).

References[1] Patent: US2010/35883, 2010, A1. Location in patent: Page/Page column 48
[2] Patent: WO2011/130661, 2011, A1. Location in patent: Page/Page column 84-85
[3] Journal fuer Praktische Chemie/Chemiker-Zeitung, 1993, vol. 335, # 1, p. 17 - 22
[4] Advanced Synthesis and Catalysis, 2010, vol. 352, # 11-12, p. 1834 - 1840
[5] Chemistry - A European Journal, 2011, vol. 17, # 21, p. 5903 - 5907
4-Aminophthalide Preparation Products And Raw materials
Raw materials4-Nitrophthalide-->Ethyl acetate-->Hydrogen
Tag:4-Aminophthalide(59434-19-4) Related Product Information
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