1,3-Benzenedicarboxaldehyde, 5-[(1R)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-
Macrocarpal I
CAS: 179388-54-6
Molecular Formula: C28H42O7
1,3-Benzenedicarboxaldehyde, 5-[(1R)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy- - Names and Identifiers
1,3-Benzenedicarboxaldehyde, 5-[(1R)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy- - Physico-chemical Properties
| Molecular Formula | C28H42O7 |
| Molar Mass | 490.63 |
| Density | 1.226±0.06 g/cm3(Predicted) |
| Boling Point | 569.5±50.0 °C(Predicted) |
| Specific Rotation(α) | -49.1 (c, 0.028 in EtOH) |
| Appearance | Pale yellow powder |
| pKa | 5.40±0.50(Predicted) |
| Storage Condition | 2-8℃ |
1,3-Benzenedicarboxaldehyde, 5-[(1R)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy- - Reference
| Reference Show more | 1. Lu Qi, Ying Zhang, Wenjuan Zhang, Yiqing Wang, Yue Han, Yanqing Ding, The inhibition of colorectal cancer growth by the natural product macrocarpal I, Free Radical Biology and Medicine, Volume 162, 2021, Pages 383-391, ISSN 0891-5849, https://doi.org/10.10 2. [IF=6.17] Lu Qi et al."The inhibition of colorectal cancer growth by the natural product macrocarpal I."Free Radical Bio Med. 2021 Jan;162:383 |
1,3-Benzenedicarboxaldehyde, 5-[(1R)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy- - Introduction
Macrocarpal I(Macrocarpal I) is a natural organic compound with a special chemical structure. It is extracted from the root bark of the large-fruited Eucalyptus (Eucalyptus macrocarpa).
Properties of Macrocarpal I:
Macrocarpal I is a colorless or slightly yellow oily liquid. It has a strong aromatic odor, is soluble in organic solvents such as ethanol and dimethyl methanol, and is almost insoluble in water.
Use of Macrocarpal I:
Macrocarpal I has a variety of applications in the pharmaceutical and flavor industries. It is widely used as an ingredient in flavors and can be used to blend floral and fruit-scented products. In addition, it also has biological activities such as antioxidant, antibacterial and anti-inflammatory, so it is also studied and used in the field of drug development.
preparation of Macrocarpal I:
Macrocarpal I is mainly obtained by extracting from the root bark of Eucalyptus Macrocarpal. The extraction method is usually a solvent extraction method, using an appropriate organic solvent such as ethanol or dimethyl methanol, and soaking or heating extraction of the root bark of Eucalyptus macrophylla with a solvent. Macrocarpal I is then purified by distillation or extraction.
Safety information for Macrocarpal I:
Based on the current information, Macrocarpal I is considered safe for general use. However, like other chemicals, it may cause an allergic or irritant reaction in some people. Before use, skin sensitivity test should be carried out first, and appropriate use concentration and safety operation should be followed.
Properties of Macrocarpal I:
Macrocarpal I is a colorless or slightly yellow oily liquid. It has a strong aromatic odor, is soluble in organic solvents such as ethanol and dimethyl methanol, and is almost insoluble in water.
Use of Macrocarpal I:
Macrocarpal I has a variety of applications in the pharmaceutical and flavor industries. It is widely used as an ingredient in flavors and can be used to blend floral and fruit-scented products. In addition, it also has biological activities such as antioxidant, antibacterial and anti-inflammatory, so it is also studied and used in the field of drug development.
preparation of Macrocarpal I:
Macrocarpal I is mainly obtained by extracting from the root bark of Eucalyptus Macrocarpal. The extraction method is usually a solvent extraction method, using an appropriate organic solvent such as ethanol or dimethyl methanol, and soaking or heating extraction of the root bark of Eucalyptus macrophylla with a solvent. Macrocarpal I is then purified by distillation or extraction.
Safety information for Macrocarpal I:
Based on the current information, Macrocarpal I is considered safe for general use. However, like other chemicals, it may cause an allergic or irritant reaction in some people. Before use, skin sensitivity test should be carried out first, and appropriate use concentration and safety operation should be followed.
Last Update：2024-04-09 20:45:29
![1,3-Benzenedicarboxaldehyde, 5-[(1R)-1-[(1S,4R,4aR,6R,8aS)-decahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-1-naphthalenyl]-3-methylbutyl]-2,4,6-trihydroxy-](http://res.chembk.com/assets/str/2d/1/17/179388-54-6.png)
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CAS: 179388-54-6
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