4-Benzofurazancarboxaldehyde

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CAS:32863-32-4
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Products Intro: Product Name:benzo[c][1,2,5]oxadiazole-4-carbaldehyde
CAS:32863-32-4
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CAS:32863-32-4
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4-Benzofurazancarboxaldehyde manufacturers

4-Benzofurazancarboxaldehyde Basic information
Product Name:4-Benzofurazancarboxaldehyde
Synonyms:2,1,3-Benzoxadiazole-4-carboxaldehyde (9CI);2,1,3-BENZOXADIAZOLE-4-CARBOXALDEHYDE;2,1,3-Benzoxadiazole-4-carbaldehyde;4-Benzofurazone Carboxaldehyde;2,1,3-Benzoxadiazole-4-aldehyde;Benzofurazon-4-Carboxaldehyde;4-FORMYL-BENZO[C][1,2,5]OXADIAZOLE;4-Benzofurazancarboxaldehyde ,97%
CAS:32863-32-4
MF:C7H4N2O2
MW:148.12
EINECS:682-565-9
Product Categories:Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;ALDEHYDE
Mol File:32863-32-4.mol
4-Benzofurazancarboxaldehyde Structure
4-Benzofurazancarboxaldehyde Chemical Properties
Melting point 100-102°C
Boiling point 277 °C
density 1.417
Fp 121 °C
storage temp. Inert atmosphere,2-8°C
solubility Dichloromethane (Slightly), Chloroform (Slightly), Methanol (Slightly)
form Solid
pka-1.86±0.45(Predicted)
color Light Brown
InChIInChI=1S/C7H4N2O2/c10-4-5-2-1-3-6-7(5)9-11-8-6/h1-4H
InChIKeyYBBRQAXNTWMMFZ-UHFFFAOYSA-N
SMILESN1=C2C=CC=C(C=O)C2=NO1
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HazardClass IRRITANT
HS Code 2934999090
MSDS Information
4-Benzofurazancarboxaldehyde Usage And Synthesis
Chemical PropertiesLight Brown Solid
UsesA synthetic intermediate for the production of Isradipine.
Synthesis
4-(BROMOMETHYL)-2,1,3-BENZOXADIAZOLE

32863-30-2

4-Benzofurazancarboxaldehyde

32863-32-4

General procedure for the synthesis of benzodiazole-4-carbaldehyde from 4-(bromomethyl)benzo[c][1,2,5]oxadiazole: 4-(bromomethyl)benzo[c][1,2,5]oxadiazole (19.7 g, 0.1 mol), dimethylsulfoxide (DMSO, 15 mL), and sodium bicarbonate (10 g, 0.12 mol) were added to the reaction flask sequentially. The reaction mixture was heated to 100-150 °C under nitrogen protection. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently extracted with deionized water and ethyl acetate. The organic layers were combined and washed with saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent to give 10.6 g of a light yellow solid product in 71.6% yield with a melting point of 108-109 °C.

References[1] Patent: CN102285978, 2016, B. Location in patent: Paragraph 0031
[2] European Journal of Medicinal Chemistry, 1996, vol. 31, # 1, p. 3 - 10
Tag:4-Benzofurazancarboxaldehyde(32863-32-4) Related Product Information
5-(BROMOMETHYL)-2,1,3-BENZOXADIAZOLE Isopropyl 3-aminocrotonate 4-Methylbenzofurazan 3-oxid Methyl 3-aminocrotonate m-Phthalaldehyde Terephthalaldehyde 1-Nonanal 4-METHYL-BENZO(1,2,5)OXADIAZOLE o-Phthalaldehyde Paraldehyde Albendazole 2,1,3-Benzothiadiazole Benzo[b]thien-2-ylboronic acid Formyl radical 4-Benzofurazancarboxaldehyde DIHYDROXY BENZALDEHYDE phenyldimethanal BUTTPARK 37\04-04

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