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ChemicalBook >  Product Catalog >  Organic Chemistry >  Alcohols,Phenols,Phenol alcohols >  2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL

2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL

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2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL Basic information

Product Name:
2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL
Synonyms:
  • RARECHEM AL BD 0202
  • 3,4-ETHYLENEDIOXYBENZYL ALCOHOL
  • 2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL
  • 2,3-dihydro-1,4-benzodioxin-6-methanol
  • 6-(Hydroxymethyl)-2,3-dihydro-1,4-benzodioxin
  • (2,3-dihydrobenzo[b][1,4]dioxin-6-yl)methanol
  • 2,3-Dihydro-6-(hydroxymethyl)-1,4-benzodioxine
  • (2,3-Dihydro-benzo[1,4]dioxin-6-yl)-Methanol
CAS:
39270-39-8
MF:
C9H10O3
MW:
166.17
EINECS:
254-396-7
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
Mol File:
39270-39-8.mol
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2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL Chemical Properties

Boiling point:
129 °C
Density 
1.257±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
14.25±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-51-41-37/38
Safety Statements 
26-36/37/39-39
HazardClass 
IRRITANT
HS Code 
2932990090

MSDS

  • Language:English Provider:ALFA
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2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL Usage And Synthesis

Synthesis

29668-44-8

39270-39-8

General procedure for the synthesis of benzodioxane-6-methanol from 1,4-benzodioxane-6-carboxaldehyde: 2,3-Dihydro-benzo[1,4]dioxine-6-carboxaldehyde [RN 29668-44-8] (3.04 g, 18.54 mmol) was dissolved in ethanol (100 mL) and the solution was cooled to 0 °C. Sodium borohydride (1.41 g, 37.77 mmol) was added to this solution in batches with stirring. The reaction mixture was continued to be stirred at room temperature for 1 hour. Upon completion of the reaction, the reaction was quenched by the slow addition of water (10 mL), followed by concentration under reduced pressure to remove the solvent. The residue was separated by extraction with 5% aqueous sodium bicarbonate (20 mL) and dichloromethane (2 x 50 mL). The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography using a gradient elution of dichloromethane and methanol. Benzodioxane-6-methanol was finally obtained as a colorless oil (3.00 g, 97% yield).

References

[1] Patent: WO2003/87098, 2003, A1. Location in patent: Page/Page column 43
[2] Patent: WO2010/83246, 2010, A1. Location in patent: Page/Page column 149-150
[3] Australian Journal of Chemistry, 1984, vol. 37, # 4, p. 893 - 901
[4] Chemical Communications (Cambridge, United Kingdom), 2018, vol. 54, # 83, p. 11805 - 11808
[5] Tetrahedron, 2001, vol. 57, # 39, p. 8297 - 8303

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