Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Aromatic aldehydes >  2-ALLYLOXYBENZALDEHYDE

2-ALLYLOXYBENZALDEHYDE

Basic information Safety Supplier Related

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
More
Less

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
Flash point:
109 °C
storage temp. 
Inert atmosphere,2-8°C
form 
clear liquid
color 
Colorless to Light yellow to Light orange
Specific Gravity
1.079
Sensitive 
Air Sensitive
InChIKey
BXCJDECTRRMSCV-UHFFFAOYSA-N
CAS DataBase Reference
28752-82-1(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/38
Safety Statements 
37/39-26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29124900

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
More
Less

2-ALLYLOXYBENZALDEHYDE Usage And Synthesis

Chemical Properties

clear yellow to orange liquid

Synthesis

90-02-8

106-95-6

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

2-ALLYLOXYBENZALDEHYDESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com