1,3-Cyclopentanedicarboxylic acid
cyclopentane-1,3-dicarboxylic acid
CAS: 4056-78-4
Molecular Formula: C7H10O4
1,3-Cyclopentanedicarboxylic acid - Names and Identifiers
| Name | cyclopentane-1,3-dicarboxylic acid |
| Synonyms | NORCAMPHORICACID Norcamphoric acid 1,3-Cyclopentanedicarboxylic acid Cyclopentane-1,3-dicarboxylic acid cyclopentane-1,3-dicarboxylic acid (1R,3S)-cyclopentane-1,3-dicarboxylic acid |
| CAS | 4056-78-4 |
| InChI | InChI=1/C7H10O4/c8-6(9)4-1-2-5(3-4)7(10)11/h4-5H,1-3H2,(H,8,9)(H,10,11)/t4-,5+ |
1,3-Cyclopentanedicarboxylic acid - Physico-chemical Properties
| Molecular Formula | C7H10O4 |
| Molar Mass | 158.15 |
| Density | 1.396±0.06 g/cm3(Predicted) |
| Melting Point | 121.5 °C |
| Boling Point | 320.7±25.0 °C(Predicted) |
| Flash Point | 161.9°C |
| Vapor Presure | 6.51E-05mmHg at 25°C |
| pKa | 4.23±0.40(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.535 |
1,3-Cyclopentanedicarboxylic acid - Introduction
cyclopentane-1,3-dicarboxylic acid is an organic compound with the chemical formula C7H10O4. The following is a description of some of the properties, uses, preparation and safety information of the compound:
Nature:
cyclopentane-1,3-dicarboxylic acid is a colorless crystal, soluble in water and some organic solvents. It is acidic and can react with bases to form the corresponding salts. In addition, it can also occur esterification, acylation and other common organic reactions.
Use:
cyclopentane-1,3-dicarboxylic acid has certain uses in chemical research, organic synthesis and industry. It can be used as an intermediate in organic synthesis for the synthesis of other organic compounds. In addition, it can also be used to prepare homopolyester resins and coatings, as a raw material for plasticizers, catalysts and stabilizers.
Preparation Method:
cyclopentane-1,3-dicarboxylic acid can be synthesized by a variety of methods. A common method is obtained by oxidative synthesis reaction, that is, cyclopentene is reacted with acidic hydrogen peroxide to produce cyclopentane-1,3-dicarboxylic acid. In addition, it can also be produced by an oxidation-reduction reaction of cyclopentanone.
Safety Information:
cyclopentane-1,3-dicarboxylic acid is generally a low-toxic compound under conventional laboratory conditions, but it is still necessary to pay attention to compliance with experimental safety procedures. During the operation, avoid contact with skin and eyes, and ensure good ventilation. If ingested or inhaled, seek medical help immediately. In addition, the compound should be kept dry during storage and transportation, avoiding contact with strong oxidizing agents.
Nature:
cyclopentane-1,3-dicarboxylic acid is a colorless crystal, soluble in water and some organic solvents. It is acidic and can react with bases to form the corresponding salts. In addition, it can also occur esterification, acylation and other common organic reactions.
Use:
cyclopentane-1,3-dicarboxylic acid has certain uses in chemical research, organic synthesis and industry. It can be used as an intermediate in organic synthesis for the synthesis of other organic compounds. In addition, it can also be used to prepare homopolyester resins and coatings, as a raw material for plasticizers, catalysts and stabilizers.
Preparation Method:
cyclopentane-1,3-dicarboxylic acid can be synthesized by a variety of methods. A common method is obtained by oxidative synthesis reaction, that is, cyclopentene is reacted with acidic hydrogen peroxide to produce cyclopentane-1,3-dicarboxylic acid. In addition, it can also be produced by an oxidation-reduction reaction of cyclopentanone.
Safety Information:
cyclopentane-1,3-dicarboxylic acid is generally a low-toxic compound under conventional laboratory conditions, but it is still necessary to pay attention to compliance with experimental safety procedures. During the operation, avoid contact with skin and eyes, and ensure good ventilation. If ingested or inhaled, seek medical help immediately. In addition, the compound should be kept dry during storage and transportation, avoiding contact with strong oxidizing agents.
Last Update：2024-04-10 22:29:15
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