86319-80-4

Basic information

• Product Name: 1,3-Benzodioxole-4,7-diol
• Synonyms: 1,3-Benzodioxole-4,7-diol
• CAS NO: 86319-80-4
• Molecular Formula: C7H6O4
• Molecular Weight: 154.12
• Mol File: 86319-80-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 324.9±42.0 °C(Predicted)
• Appearance: /
• Density: 1.581±0.06 g/cm3(Predicted)
• PKA: 10.02±0.20(Predicted)
• CAS DataBase Reference: 1,3-Benzodioxole-4,7-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzodioxole-4,7-diol(86319-80-4)
• EPA Substance Registry System: 1,3-Benzodioxole-4,7-diol(86319-80-4)

Safety Data

• Hazardous Substances Data: 86319-80-4(Hazardous Substances Data)

Usage

Chemical structure

A dihydroxybenzene derivative with two hydroxyl groups attached to a benzene ring

Functional groups

Hydroxyl groups (-OH)

Applications

a. Intermediate in the synthesis of pharmaceuticals and agrochemicals
b. Potential antioxidant and anti-inflammatory properties
c. Research for use in the development of new materials
d. Research for use in environmental remediation processes

Physical state

Likely a solid or liquid, depending on temperature (not specified in the material)

Solubility

Not specified in the material, but may be soluble in organic solvents due to its hydrocarbon backbone

Reactivity

Reacts with other chemicals to form pharmaceuticals, agrochemicals, and other materials

Safety

Potential hazards and safety precautions not specified in the material, but should be handled with care due to its use in chemical synthesis and potential biological activity

Environmental impact

Being researched for use in environmental remediation processes, suggesting it may have a role in addressing environmental issues

Upstream product

• 23731-75-1 1,4-dimethoxy-2,3-methylenedioxybenzene 
• 109765-60-8 2,3-dihydroxy-1,4-dimethoxybenzene 
• 21450-56-6 1,2,3,4-tetramethoxybenzene 
• 19676-64-3 2,3,4-trimethoxyphenol 
• 2103-57-3 2,3,4-trimethoxybenzaldehyde 
• 610-02-6 2,3,4-trihydroxybenzoic acid 
• 4776-00-5 4-hydroxybenzo[d][1,3]dioxole-5-carboxylic acid 
• 115943-52-7 4-(phenylmethoxy)-1,3-benzodioxole 
• 115943-53-8 4-formyl-7-(phenylmethoxy)-1,3-benzodioxole 
• 115943-54-9 4-hydroxy-7-(phenylmethoxy)-1,3-benzodioxole 
• 69393-72-2 2H-benzo[d][1,3]dioxolan-4-ol 

Downstream Products

• 86319-72-4 2,3-methylenedioxy-1,4-benzoquinone 

Relevant articles and documents

Synthesis of isoflavones by tandem demethylation and ring-opening/cyclization of methoxybenzoylbenzofurans

The unexpected conversion of benzoylbenzofurans into isoflavones through an intramolecular cascade that involves deprotection and ring-opening/cyclization is described. This was discovered in an investigation of the possible transformation of benzoylbenzofurans into coumaronochromones. This route affords isoflavones in two major steps from acetophenones and benzoquinones. The transformation was validated by synthesizing differently substituted isoflavone derivatives and further applied to a concise synthesis of a potential anticancer lead compound, glaziovianin A (1).

Derivatives of 1,3-Benzdioxoles, 48. Preparation and Reactions of 1,3-Benzdioxole-4,7-quinones

We describe the preparation of a substituted 1,3-benzdioxole-4,7-quinone complex (2) by reaction of 4-hydroxy-1,3-benzdioxole (1) with potassiumnitrosodisulfonate.The quinones 4a-d can be obtained by treatment of the 4-hydroxy-7-methoxy-1,3-benzdioxoles 3a-d with ammoniumcerium(IV)nitrate.Reaction of 2 with several cyclophiles gives the addition compounds resp. the dehydrogenation-products 6b-d in partly high yields. - Keywords: 1,3-Benzdioxol-4,7-chinon, 6,7-Dimethyl-naphtho-1,3-dioxol-4,9-chinon, 6-Hydroxy-naphtho-1,3-dioxol-4,9-chinon