1,3-Dihydroisobenzofuran-5-ylamine

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Products Intro: Product Name:1,3-Dihydroisobenzofuran-5-ylamine
CAS:61964-08-7
Purity:99% Package:100kg;2USD|10kg;4USD|1kg;6USD
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Products Intro: Product Name:5-Amino-1,3-dihydrobenzo[c]furan
CAS:61964-08-7
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Products Intro: Product Name:1,3-Dihydroisobenzofuran-5-amine
CAS:61964-08-7
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Products Intro: Product Name:1,3-dihydro-2-benzofuran-5-amine
CAS:61964-08-7
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Products Intro: Product Name:1,3-Dihydroisobenzofuran-5-ylamine
CAS:61964-08-7
Purity:98% Package:1g;1.3USD

1,3-Dihydroisobenzofuran-5-ylamine manufacturers

1,3-Dihydroisobenzofuran-5-ylamine Basic information
Product Name:1,3-Dihydroisobenzofuran-5-ylamine
Synonyms:1,3-DIHYDROISOBENZOFURAN-5-AMINE;4-PHENYLPHTHALONITRILE;1,3-Dihydro-2-benzofuran-5-amine;5-Amino-1,3-dihydro-2-benzo[c]furan;5-Isobenzofuranamine,1,3-dihydro-;1,3-Dihydroisobenzofuran-5-ylamine;5-Amino-1,3-dihydrobenzo[c]furan;1,3-dihydro-2-benzofuran-5-amine(SALTDATA: FREE)
CAS:61964-08-7
MF:C8H9NO
MW:135.16
EINECS:
Product Categories:
Mol File:61964-08-7.mol
1,3-Dihydroisobenzofuran-5-ylamine Structure
1,3-Dihydroisobenzofuran-5-ylamine Chemical Properties
Melting point 104-105 °C
Boiling point 295.9±40.0 °C(Predicted)
density 1.208±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka4.79±0.20(Predicted)
InChIInChI=1S/C8H9NO/c9-8-2-1-6-4-10-5-7(6)3-8/h1-3H,4-5,9H2
InChIKeyGKULNTLNUHOMGD-UHFFFAOYSA-N
SMILESC1C2=C(C=C(N)C=C2)CO1
Safety Information
HS Code 2932990090
MSDS Information
1,3-Dihydroisobenzofuran-5-ylamine Usage And Synthesis
Synthesis
5-Nitro-1,3-dihydroisobenzofuran

52771-99-0

1,3-Dihydroisobenzofuran-5-ylamine

61964-08-7

Step 2: 5-Nitro-1,3-dihydroisobenzofuran (compound 8, 5.63 g, 34.1 mmol) was dissolved in 56 mL of ethanol. To this solution was added tin chloride dihydrate (23.1 g, 102 mmol). The reaction mixture was stirred at 70°C for 1 hour. After completion of the reaction, it was cooled to room temperature and water and 2 mol/L aqueous sodium hydroxide solution were added sequentially to adjust the pH to 7. The reaction mixture was extracted with ethyl acetate and the organic layer was washed with brine. The organic phase was concentrated under reduced pressure to afford 4.6 g of crude product of 1,3-dihydroisobenzofuran-5-amine (compound 9) in 98% yield. The product was characterized by 1H-NMR (CDCl3): δ 3.71 (br s, 2H), 5.02 (s, 4H), 6.57 (s, 1H), 6.60 (dd, J = 7.9,2.0 Hz, 1H), 7.01 (d, J = 7.9 Hz, 1H).

References[1] Patent: EP3287443, 2018, A1. Location in patent: Paragraph 0585; 0587
[2] Patent: US4144341, 1979, A
1,3-Dihydroisobenzofuran-5-ylamine Preparation Products And Raw materials
Raw materials5-Nitro-1,3-dihydroisobenzofuran-->Ethanol
Tag:1,3-Dihydroisobenzofuran-5-ylamine(61964-08-7) Related Product Information
2,3-Dihydrofuran Phthalan Tetrahydrofuran Dihydromyrcenol Benzofuran 2,3-Dihydrobenzofuran Bis(2-ethylhexyl)amine Triallylamine Dibenzylamine POLY(TETRAHYDROFURAN) STANDARD 20000 1,3-Dihydroisobenzofuran-5-ylamine

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