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4-Morpholinobenzaldehyde

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Products Intro: Product Name:4-(4-Morpholinyl)benzaldehyde
CAS:1204-86-0
Purity:98% Min. Package:1G;1KG;100KG
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Products Intro: Product Name:4-Morpholinobenzaldehyde
CAS:1204-86-0
Purity:0.98 Package:25KG;5KG;1KG Remarks:Mature product
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:4-Morpholin-4-yl-benzaldehyde
CAS:1204-86-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-70285
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Products Intro: Product Name:4-Morpholin-4-yl-benzaldehyde
CAS:1204-86-0
Purity:0.98 Package:1g;5g;25g;100;500g
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:4-morpholinobenzaldehyde
CAS:1204-86-0
Purity:0.99 Package:1kg

4-Morpholinobenzaldehyde manufacturers

4-Morpholinobenzaldehyde Basic information
Product Name:4-Morpholinobenzaldehyde
Synonyms:AKOS BC-2976;AKOS BBS-00004794;4-(4-FORMYLPHENYL)MORPHOLINE;4-(4-MORPHOLINYL)BENZALDEHYDE;4-MORPHOLIN-4-YL-BENZALDEHYDE;4-MORPHOLINOBENZALDEHYDE;4-MORPHOLINOBENZENECARBALDEHYDE;IFLAB-BB F1274-0239
CAS:1204-86-0
MF:C11H13NO2
MW:191.23
EINECS:
Product Categories:Carbonyl Compounds;Heterocycles;pharmacetical;API intermediates
Mol File:1204-86-0.mol
4-Morpholinobenzaldehyde Structure
4-Morpholinobenzaldehyde Chemical Properties
Melting point 65-69 °C
Boiling point 365.5±37.0 °C(Predicted)
density 1.163±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
pka1.87±0.40(Predicted)
form powder to crystal
color Light yellow to Yellow to Orange
CAS DataBase Reference1204-86-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39-24/25
WGK Germany 3
HazardClass IRRITANT
HS Code 29349990
MSDS Information
4-Morpholinobenzaldehyde Usage And Synthesis
Uses4-Morpholinobenzaldehyde is mainly used as a raw material for organic synthesis. It can be used to prepare dihydrotetrazolopyrimidine derivatives (ethyl 5-methyl-7-(4-morpholinophenyl)-4,7-dihydrotetrazolo[1,5-a]pyrimidine-6-carboxylate), coumarin-based chalcone derivatives ((E)-3-[3-(4-(4-morpholinophenyl)acryloyl]-2H-chromen-2-one) and Ru(II) polypyridine complexes, among others.
Synthesis
Morpholine

110-91-8

4-Fluorobenzaldehyde

459-57-4

4-Morpholinobenzaldehyde

1204-86-0

General procedure for the synthesis of 4-(4-morpholine)benzaldehyde from morpholine and p-fluorobenzaldehyde: In a dry reaction flask, p-fluorobenzaldehyde (25.0 g, 0.200 mol), morpholine (0.300 mol), and anhydrous potassium carbonate (40.0 g) were dissolved in N,N-dimethylformamide (DMF, 300 mL), and a catalytic amount of Aliquat 336 reagent. The reaction mixture was stirred at reflux for 24 hours at 100°C. Upon completion of the reaction, the mixture was concentrated to dryness under reduced pressure and cooled to room temperature. Subsequently, the concentrate was slowly poured into ice water and allowed to stand overnight. The precipitated solid was collected by filtration, washed with water and recrystallized with methanol to afford the target compound 4-morpholino benzaldehyde (Id) in 89% yield as yellow crystals with a melting point of 69 °C (in agreement with literature reports) [49,50].

References[1] Journal of Medicinal Chemistry, 2016, vol. 59, # 6, p. 2747 - 2759
[2] Bioorganic Chemistry, 2014, vol. 57, p. 65 - 82
[3] European Journal of Medicinal Chemistry, 2018, vol. 144, p. 68 - 81
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 12, p. 3721 - 3725
[5] Russian Journal of General Chemistry, 2013, vol. 83, # 10, p. 1864 - 1868
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