1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy-, also known as 5-hydroxy-1,2,3,4-benzenetetracarboxylic acid, is an organic compound with the chemical formula C10H6O9. It is a derivative of benzene with four carboxylic acid groups and a hydroxyl group attached to the central carbon atom. 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy- is a white crystalline solid and is soluble in water. It is an important intermediate in the synthesis of various dyes, pigments, and pharmaceuticals. The compound is also known for its potential applications in the field of materials science, such as in the production of conductive polymers and as a precursor for the synthesis of complex organic molecules. Its unique structure and properties make it a valuable compound for research and industrial applications.
4961-06-2
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Basic information
- Product Name: 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy-
- Synonyms: 5-Hydroxy-benzene-1,2,3,4-tetracarboxylic acid;Hydroxy-benzol-1,2,3,4-tetracarbonsaeure;Phenol-tetracarbonsaeure-(2.3.4.5);5-Hydroxy-1,2,3,4-benzenetetracarboxylicsaeure;
- CAS NO:4961-06-2
- Molecular Formula: C10H6O9
- Molecular Weight: 270.152
- EINECS: N/A
- Product Categories: N/A
- Mol File: 4961-06-2.mol
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Chemical Properties
- Melting Point: 241 - 243 °C
- Boiling Point: 612.7±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: N/A
- Density: 1.957±0.06 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy-(CAS DataBase Reference)
- NIST Chemistry Reference: 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy-(4961-06-2)
- EPA Substance Registry System: 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy-(4961-06-2)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 4961-06-2(Hazardous Substances Data)
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4961-06-2 Usage
Explanation
1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxyis derived from benzenetetracarboxylic acid by attaching a hydroxy group (-OH) at the 5th position.Explanation
The hydroxy group is attached to the 5th position of the benzene ring, making it a 5-hydroxy derivative.4. Precursor in synthesis
Explanation
1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy- is used as a starting material for the synthesis of various pharmaceuticals and organic compounds.Explanation
Due to its versatile structure, 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxyhas potential applications in different fields, including the development of new drugs, materials, and organic chemical reactions.6. Versatile building block
Explanation
The presence of the hydroxy group in 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy- allows it to be a versatile building block for the synthesis of more complex chemical structures.7. Important intermediate
Explanation
As a result of its versatility, 1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxyis an important intermediate in the production of a wide range of chemical products.Hydroxy group attachment
5th positionApplications
Medicine, materials science, and organic chemistryCheck Digit Verification of cas no
The CAS Registry Mumber 4961-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.Calculate Digit Verification of CAS Registry Number 4961-06:
(6*4)+(5*9)+(4*6)+(3*1)+(2*0)+(1*6)=102
102 % 10 = 2
So 4961-06-2 is a valid CAS Registry Number.
4961-06-2Upstream product
4961-06-2Downstream Products
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1,2,3,4-Benzenetetracarboxylic acid, 5-hydroxy-
