1,3-Benzodioxole, 99%
1,3-Benzodioxole, 99%
1,3-Benzodioxole, 99%
Thermo Scientific Chemicals

1,3-Benzodioxole, 99%

CAS: 274-09-9 | C7H6O2 | 122.123 g/mol
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Catalog number A14192.30
also known as A14192-30
Price (USD)
200.00
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Quantity:
250 g
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Price (USD)
200.00
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Chemical Identifiers
CAS274-09-9
IUPAC Name2H-1,3-benzodioxole
Molecular FormulaC7H6O2
InChI KeyFTNJQNQLEGKTGD-UHFFFAOYSA-N
SMILESC1OC2=CC=CC=C2O1
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SpecificationsSpecification SheetSpecification Sheet
Refractive Index1.5370-1.5410 @ 20°C
FormLiquid
Appearance (Color)Clear colorless to yellow to orange
Assay (GC)≥98.5%
CommentMay darken on storage
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1,3-Benzodioxole is useful in gemological stimulant detection. It is also used as a precursor for perfumes, photo initiators, agrochemicals and pharmaceuticals.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,3-Benzodioxole is useful in gemological stimulant detection. It is also used as a precursor for perfumes, photo initiators, agrochemicals and pharmaceuticals.

Solubility
Soluble in water (2g/L).

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only

General References:

  1. Corwin Hansch. Use of homolytic, steric, and hydrophobic constants in a structure-activity study of 1,3-benzodioxole synergists. J. Med. Chem. 1968, 11 (5), 920-924.
  2. Ana Cristina Lima Leite; Kezia Peixoto da Silva; Ivone A. de Souza; Janete Magali de Araújo; Dalci José Brondani. Synthesis, antitumour and antimicrobial activities of new peptidyl derivatives containing the 1,3-benzodioxole system. European Journal of Medicinal Chemistry. 2004, 39 (12), 1059-1065.