D-gulo-Heptonic acid, 3,7-anhydro-2-deoxy-7-C-phenyl-, δ-lactone, (7S)-
Goniopypyrone
CAS: 129578-07-0
Molecular Formula: C13H14O5
D-gulo-Heptonic acid, 3,7-anhydro-2-deoxy-7-C-phenyl-, δ-lactone, (7S)- - Names and Identifiers
D-gulo-Heptonic acid, 3,7-anhydro-2-deoxy-7-C-phenyl-, δ-lactone, (7S)- - Physico-chemical Properties
| Molecular Formula | C13H14O5 |
| Molar Mass | 250.25 |
| Density | 1.410±0.06 g/cm3(Predicted) |
| Melting Point | 179-182 °C |
| Boling Point | 547.4±50.0 °C(Predicted) |
| Specific Rotation(α) | +54 (c, 0.4 in EtOH) |
| Appearance | Lens. |
| pKa | 12.71±0.60(Predicted) |
| Storage Condition | 2-8℃ |
D-gulo-Heptonic acid, 3,7-anhydro-2-deoxy-7-C-phenyl-, δ-lactone, (7S)- - Introduction
Goniopyrane is a natural product that belongs to a class of compounds called terpenoids. It was originally isolated from the aquatic plant Goniopyton sp. The molecular formula of Goniopyrane is C11H6O4, which has a series of special chemical properties.
Goniopyrane is a compound with a protective ring, which can be stable under the action of light and oxygen, so it has certain value in scientific research and application. It has a variety of applications in chemistry and herbal medicine.
Goniopyrane has antioxidant and antibacterial activities and can be used as a potential natural fungicide in skin care products and pharmaceutical preparations. It also promotes wound healing and anti-inflammatory effects, and can be used in fields such as surgery and drug development.
The method of preparing Goniopyrane usually involves extracting and purifying natural products obtained from Goniopyton sp. Extraction may be by solvent extraction, such as methanol or ethanol. Goniopyrane is then obtained in higher purity by a series of chemical separation and purification techniques, such as chromatography and crystallization.
Regarding the safety of Goniopyrane, because it is a natural product, no research results on its toxicity or harm have been reported. However, the use of high-purity Goniopyrane is still required to follow appropriate laboratory practices and personal protective measures to ensure safe operation.
To sum up, Goniopyrane is a natural product with antioxidant and antibacterial activity, which can be used in skin care products, drug development and surgery. Its preparation methods include extraction and purification, and safety aspects need to follow appropriate laboratory operations and personal protective measures.
Goniopyrane is a compound with a protective ring, which can be stable under the action of light and oxygen, so it has certain value in scientific research and application. It has a variety of applications in chemistry and herbal medicine.
Goniopyrane has antioxidant and antibacterial activities and can be used as a potential natural fungicide in skin care products and pharmaceutical preparations. It also promotes wound healing and anti-inflammatory effects, and can be used in fields such as surgery and drug development.
The method of preparing Goniopyrane usually involves extracting and purifying natural products obtained from Goniopyton sp. Extraction may be by solvent extraction, such as methanol or ethanol. Goniopyrane is then obtained in higher purity by a series of chemical separation and purification techniques, such as chromatography and crystallization.
Regarding the safety of Goniopyrane, because it is a natural product, no research results on its toxicity or harm have been reported. However, the use of high-purity Goniopyrane is still required to follow appropriate laboratory practices and personal protective measures to ensure safe operation.
To sum up, Goniopyrane is a natural product with antioxidant and antibacterial activity, which can be used in skin care products, drug development and surgery. Its preparation methods include extraction and purification, and safety aspects need to follow appropriate laboratory operations and personal protective measures.
Last Update：2024-04-09 21:54:55
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View History
D-gulo-Heptonic acid, 3,7-anhydro-2-deoxy-7-C-phenyl-, δ-lactone, (7S)-
湖北消旋山莨菪碱原料药
2-CHLORO-3-(2,4-DICHLOROPHENYL)PROPANENITRILE, TECH
N-(3-氨基丙基)-n-苄基-n-甲胺
Ethanone, 1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)-, O-[(2,4-dichlorophenyl)methyl]oxime, (1Z)-
2-[2-(三氟甲基)苯基]吡咯烷
1,3-环己烷二胺(顺反异构体混合物)
1-甲基-7-(4,4,5,5-四甲基-1,3,2-二氧硼杂环戊烷-2-基)-3,4-二氢喹啉-2(1H)-酮
顺式(1s,4s)-4-吗啉代环己-1-醇
3,4-环氧环己基甲酸-3',4'-环氧环己基甲酯
湖北消旋山莨菪碱原料药
2-CHLORO-3-(2,4-DICHLOROPHENYL)PROPANENITRILE, TECH
N-(3-氨基丙基)-n-苄基-n-甲胺
Ethanone, 1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)-, O-[(2,4-dichlorophenyl)methyl]oxime, (1Z)-
2-[2-(三氟甲基)苯基]吡咯烷
1,3-环己烷二胺(顺反异构体混合物)
1-甲基-7-(4,4,5,5-四甲基-1,3,2-二氧硼杂环戊烷-2-基)-3,4-二氢喹啉-2(1H)-酮
顺式(1s,4s)-4-吗啉代环己-1-醇
3,4-环氧环己基甲酸-3',4'-环氧环己基甲酯