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2-ALLYLOXYBENZALDEHYDE

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CAS:28752-82-1
Purity:99%
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CAS:28752-82-1
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2-ALLYLOXYBENZALDEHYDE manufacturers

  • 2-Allyloxybenzaldehyde
  • 2-Allyloxybenzaldehyde pictures
  • $0.00 / 10g
  • 2026-02-02
  • CAS:28752-82-1
  • Min. Order: 10mg
  • Purity: 99%HPLC
  • Supply Ability: 2000tons
  • 2-ALLYLOXYBENZALDEHYDE
  • 2-ALLYLOXYBENZALDEHYDE pictures
  • $15.00 / 1KG
  • 2021-08-11
  • CAS:28752-82-1
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
2-ALLYLOXYBENZALDEHYDE Basic information
Product Name:2-ALLYLOXYBENZALDEHYDE
Synonyms:ASISCHEM V41613;BENZALDEHYDE, 2-(2-PROPENYLOXY)-;AKOS B005827;2-ALLYLOXYBENZALDEHYDE;2-(ALLYLOXY)BENZENECARBALDEHYDE;O-ALLYLOXYBENZALDEHYDE;SALICYLALDEHYDE ALLYL ETHER;TIMTEC-BB SBB007636
CAS:28752-82-1
MF:C10H10O2
MW:162.19
EINECS:249-198-2
Product Categories:pharmacetical;Benzaldehyde;Allyl Monomers;Monomers;Polymer Science
Mol File:28752-82-1.mol
2-ALLYLOXYBENZALDEHYDE Structure
2-ALLYLOXYBENZALDEHYDE Chemical Properties
Boiling point 130 °C/10 mmHg (lit.)
density 1.079 g/mL at 25 °C (lit.)
refractive index 1.554-1.556
Fp 109 °C
storage temp. Inert atmosphere,2-8°C
form clear liquid
color Colorless to Light yellow to Light orange
Specific Gravity1.079
Sensitive Air Sensitive
InChIKeyBXCJDECTRRMSCV-UHFFFAOYSA-N
CAS DataBase Reference28752-82-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/38
Safety Statements 37/39-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29124900
MSDS Information
ProviderLanguage
ACROS English
ALFA English
2-ALLYLOXYBENZALDEHYDE Usage And Synthesis
Chemical Propertiesclear yellow to orange liquid
Synthesis
Salicylaldehyde

90-02-8

Allyl bromide

106-95-6

2-ALLYLOXYBENZALDEHYDE

28752-82-1

Salicylaldehyde (0.5 mL, 4.69 mmol, Sigma-Aldrich Catalog No. S356) was dissolved in acetonitrile (10 mL), followed by the addition of potassium carbonate (0.97 mL, 7.03 mmol) and 3-bromo-1-propene (0.45 mL, 5.16 mmol, Sigma-Aldrich Catalog No. 337528). The reaction mixture was stirred under reflux conditions for 12 hours. Upon completion of the reaction, the solvent was removed by vacuum evaporation and the residue was dissolved in ethyl acetate (5 mL). Water (10 mL) was added and stirred for 10 min at room temperature. The organic phase was separated and the aqueous layer was extracted with ethyl acetate (2 x 10 mL). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give o-propenyloxybenzaldehyde in 99% yield. The product was extracted by 1H NMR (400 MHz, CDCl3) δ= 10.25 (1H, s), 7.54-7.52 (1H, m), 7.23-7.19 (1H, m), 6.72-6.66 (2H, m), 5.82-5.75 (1H, m), 5.20-5.15 (1H, d, J = 17.6 Hz), 5.05 -5.03 (1H, d, J = 10.8 Hz), 4.33-4.31 (2H, m) ppm; 13C NMR (CDCl3) δ 188.9,160.6,135.6,132.2,127.8,124.7,120.5,117.5,112.7,68.7 ppm; Liquid Chromatography Mass Spectrometry (LCMS) m/z z (ES+) m/z: 347.0 [2M + Na]+, 185.0 [M + Na]+, 163.0 [M + H]+; Elemental Analysis: C10H10O2: Calculated value C 74.06, H 6.21; Measured value C 74.36, H 6.52.

References[1] European Journal of Medicinal Chemistry, 2010, vol. 45, # 11, p. 5265 - 5277
[2] Angewandte Chemie - International Edition, 2009, vol. 48, # 51, p. 9690 - 9692
[3] Angewandte Chemie - International Edition, 2011, vol. 50, # 26, p. 5932 - 5937
[4] Chemistry - A European Journal, 2013, vol. 19, # 47, p. 15852 - 15855
[5] Tetrahedron Letters, 1995, vol. 36, # 11, p. 1845 - 1848
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