BENZOFURAN-3-CARBALDEHYDE

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Products Intro: Product Name:benzofuran-3-carbaldehyde
CAS:4687-25-6
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CAS:4687-25-6
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Products Intro: Product Name:Benzofuran-3-carbaldehyde
CAS:4687-25-6
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Products Intro: Product Name:Benzofuran-3-carbaldehyde
CAS:4687-25-6
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Products Intro: Product Name:BENZOFURAN-3-CARBALDEHYDE
CAS:4687-25-6
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BENZOFURAN-3-CARBALDEHYDE manufacturers

BENZOFURAN-3-CARBALDEHYDE Basic information
Product Name:BENZOFURAN-3-CARBALDEHYDE
Synonyms:RARECHEM AK ML 0128;BENZOFURAN-3-CARBALDEHYDE;3-Benzofurancarbaldehyde;1-Benzofuran-3-carbaldehyde;3-Benzofurancarboxaldehyde;benzofuran-3-carbaldehyde;Benzofuran-3-carboxaldehyde;3-Formylbenzo[b]furan
CAS:4687-25-6
MF:C9H6O2
MW:146.14
EINECS:
Product Categories:API intermediate
Mol File:4687-25-6.mol
BENZOFURAN-3-CARBALDEHYDE Structure
BENZOFURAN-3-CARBALDEHYDE Chemical Properties
Melting point 39℃ (ligroine )
Boiling point 165℃ (18 Torr)
density 1.238±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form Solid
color White to yellow
Safety Information
HS Code 2932990090
MSDS Information
BENZOFURAN-3-CARBALDEHYDE Usage And Synthesis
UsesBenzofuran-3-carbaldehyde is a bioactive chemical, and can be used for the synthesis of active compound[1].
Synthesis
3-Methylbenzofuran

21535-97-7

BENZOFURAN-3-CARBALDEHYDE

4687-25-6

The general procedure for the synthesis of 3-formylbenzofuran from 3-methylbenzofuran was as follows: 3-methylbenzofuran (200 mg, 0.19 mL, 1.5 mmol) and selenium dioxide (SeO2, 200 mg, 1.8 mmol, 1.2 eq.) were suspended in 1,4-dioxane (3 mL) and heated and refluxed for 24 hours. Upon completion of the reaction, the reaction mixture was allowed to cool to room temperature, diluted with ethyl acetate/hexane (2:1 v/v, 10 mL), and filtered through a short silica gel plug to remove the selenium residue. The silica gel plugs were washed with ethyl acetate (2 x 3 mL), and the organic filtrates were combined and evaporated to dryness. Purification by silica gel column chromatography (eluent: hexane/ethyl acetate 96:4) afforded the yellow oily product 3-formylbenzofuran (162 mg, 1.1 mmol, 74% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 10.18 (s, 1H), 8.26 (s, 1H), 8.19 (m, 1H), 7.54 (m, 1H), 7.41 (m, 2H); ESI-MS m/z = 147.0 ([MH]+), calculated value C9H7O2 = 147.04.

References[1] Bolling BW, et al. Phenolic derivatives from soy flour ethanol extract are potent in vitro quinone reductase (QR) inducing agents. J Agric Food Chem. 2008 Nov 26;56(22):10473-80. DOI:10.1021/jf801541t
BENZOFURAN-3-CARBALDEHYDE Preparation Products And Raw materials
Raw materials3-Methylbenzofuran-->Selenium dioxide-->1,4-Dioxane
Preparation Products1-benzofuran-3-ylMethanaMine
Tag:BENZOFURAN-3-CARBALDEHYDE(4687-25-6) Related Product Information
ETHYL 2-METHYL-4,5,6,7-TETRAFLUOROBENZOFURAN-3-CARBOXYLATE COUMESTROL 2-Butyl-3-(4-hydroxybenzoyl)benzofuran Benzbromarone Amiodarone 3-HYDROXY-8,9-METHYLENEDIOXYCOUMESTAN Amiodarone hydrochloride 5-HYDROXY-2-METHYL-BENZOFURAN-3-CARBOXYLIC ACID 3,9-DI-O-METHYLCOUMESTROL 3-HYDROXY-9-METHOXYCOUMESTAN ETHYL 4-[(DIMETHYLAMINO)METHYL]-5-HYDROXY-2-PHENYL-1-BENZOFURAN-3-CARBOXYLATE HYDROCHLORIDE N3-(3-CHLORO-4-FLUOROPHENYL)-4,5,6,7-TETRAFLUORO-2-METHYLBENZO[B]FURAN-3-CARBOXAMIDE 5-HYDROXY-2-METHYL-BENZOFURAN-3-CARBOXYLIC ACID ETHYL ESTER 2,4-DICHLOROPHENYL 4,5,6,7-TETRAFLUORO-2-METHYLBENZO[B]FURAN-3-CARBOXYLATE 4,5,6,7-TETRAFLUORO-2-METHYL-1-BENZOFURAN-3-CARBOXYLIC ACID diethyl 2,6-dimethylfuro[2,3-f][1]benzofuran-3,7-dicarboxylate N3-[3,5-DI(TRIFLUOROMETHYL)PHENYL]-4,5,6,7-TETRAFLUORO-2-METHYLBENZO[B]FURAN-3-CARBOXAMIDE CHEMBRDG-BB 5169029

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