Basic information Safety Supplier Related

2-ALLYL-3-HYDROXYBENZALDEHYDE

Basic information Safety Supplier Related

2-ALLYL-3-HYDROXYBENZALDEHYDE Basic information

Product Name:
2-ALLYL-3-HYDROXYBENZALDEHYDE
Synonyms:
  • 3-Hydroxy-2-(prop-2-en-1-yl)benzaldehyde
  • 3-Hydroxy-2-(prop-2-en-1-yl)benzaldehyde, 2-Allyl-3-formylphenol
  • Benzaldehyde,3-hydroxy-2-(2-propen-1-yl)-
  • 2-ALLYL-3-HYDROXYBENZALDEHYDE
  • 3-hydroxy-2-prop-2-enylbenzaldehyde
CAS:
79950-42-8
MF:
C10H10O2
MW:
162.19
EINECS:
807-729-0
Mol File:
79950-42-8.mol
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2-ALLYL-3-HYDROXYBENZALDEHYDE Chemical Properties

Melting point:
102-103 °C(Solv: dichloromethane (75-09-2); hexane (110-54-3))
Boiling point:
274.4±25.0 °C(Predicted)
Density 
1.126±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder
pka
9.57±0.10(Predicted)
color 
Brown
InChI
InChI=1S/C10H10O2/c1-2-4-9-8(7-11)5-3-6-10(9)12/h2-3,5-7,12H,1,4H2
InChIKey
QVHRAGBOMUXWRI-UHFFFAOYSA-N
SMILES
C(=O)C1=CC=CC(O)=C1CC=C
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
HS Code 
2912490090
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2-ALLYL-3-HYDROXYBENZALDEHYDE Usage And Synthesis

Uses

2-Allyl-3-hydroxybenzaldehyde is useful for diastereoselective preparation of bicyclic compounds.

Synthesis

40359-32-8

79950-42-8

79950-43-9

General procedure for the synthesis of 2-allyl-3-hydroxybenzaldehyde and compounds (CAS: 79950-43-9) from 3-(allyloxy)benzaldehyde: 3-(allyloxy)benzaldehyde (308 g) and tetrahydroxynaphthalene (300 mL) were added to a 3000 mL single-necked round-bottomed flask equipped with a condenser and a thermometer. The reaction mixture was placed in a microwave reactor and slowly heated to 180-182 °C at 1500 W (ramp-up time of 5-10 min, internal temperature was monitored) and the reaction was continuously stirred for 7-8 h at this temperature. During the reaction, the color of the mixture gradually changed to brown. Upon completion of the reaction, the mixture was cooled to room temperature, followed by further cooling at 0 to 5 °C for 30 min. The solid product was collected by filtration and dried to give off-white 2-allyl-3-hydroxybenzaldehyde (145.5 g, 47% yield).

References

[1] Patent: US2016/107973, 2016, A1. Location in patent: Paragraph 0034; 0035; 0036
[2] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981, p. 2677 - 2679
[3] Organic and Biomolecular Chemistry, 2004, vol. 2, # 17, p. 2461 - 2470
[4] Synlett, 2012, vol. 23, # 6, p. 867 - 872
[5] Tetrahedron Letters, 2012, vol. 53, # 16, p. 2125 - 2128

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