485-63-2
3',4',7-Trihydroxyisoflavone
CAS: 485-63-2
Molecular Formula: C15H10O5
485-63-2 - Names and Identifiers
| Name | 3',4',7-Trihydroxyisoflavone |
| Synonyms | 3'-HYDROXYDAIDZEIN HYDROXYDAIDZEIN, 3'- MIF-TAUTOMERASE INHIBITOR I 7,3',4'-TRIHYDROXYISOFLAVONE 3',4',7-TRIHYDROXYISOFLAVONE 7,3',4'-Trihydroxyisoflavone 3',4',7-Trihydroxyisoflavone 3-(3,4-Dihydroxyphenyl)-7-hydroxy-4H-chromen-4-one 3-(3,4-dihydroxyphenyl)-7-hydroxy-4H-chromen-4-one 2,7-dihydroxy-3-(4-hydroxyphenyl)-1-benzopyran-4-one 3-(3,4-Dihydroxyphenyl)-7-hydroxy-4H-1-benzopyran-4-one 4H-1-Benzopyran-4-one, 3-(3,4-dihydroxyphenyl)-7-hydroxy- |
| CAS | 485-63-2 |
| InChI | InChI=1/C15H10O5/c16-9-2-3-10-14(6-9)20-7-11(15(10)19)8-1-4-12(17)13(18)5-8/h1-7,16-18H |
485-63-2 - Physico-chemical Properties
| Molecular Formula | C15H10O5 |
| Molar Mass | 270.24 |
| Density | 1.548±0.06 g/cm3(Predicted) |
| Melting Point | 280-282°C |
| Boling Point | 572.8±50.0 °C(Predicted) |
| Flash Point | 224°C |
| Solubility | DMF, ethanol, methanol |
| Vapor Presure | 1.01E-13mmHg at 25°C |
| Appearance | White powder |
| Color | Off-White |
| BRN | 251800 |
| pKa | 6.86±0.20(Predicted) |
| Storage Condition | -20°C Freezer |
| Stability | Store in Freezer |
| Refractive Index | 1.732 |
| MDL | MFCD00143002 |
485-63-2 - Risk and Safety
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10 |
485-63-2 - Introduction
3 ',4',7-Trihydroxyisoflavone is a naturally occurring isoflavone. Its molecular formula is C15H10O5 and its structural formula is:
OH OH
/
C=C
/
OH OH
The following are the properties of 3 ',4',7-Trihydroxyisoflavone:
1. Appearance: 3 ',4',7-Trihydroxyisoflavone is a yellow crystalline solid.
2. Solubility: It has low solubility in water and good solubility in organic solvents.
The main uses of 3 ',4',7-Trihydroxyisoflavone are as follows:
1. Antioxidant: It has strong antioxidant activity, can scavenge free radicals, protect cells from free radical damage.
2. Anti-inflammatory effect: 3 ',4',7-Trihydroxyisoflavone has inhibitory effect on inflammatory response and can be used to treat inflammation-related diseases.
3. Anticancer activity: Studies have shown that 3 ',4',7-Trihydroxyisoflavone has an inhibitory effect on certain cancer cells and may have anti-cancer potential.
The methods for preparing 3 ',4',7-Trihydroxyisoflavone mainly include natural extraction and chemical synthesis.
1. Natural extraction: 3 ',4',7-Trihydroxyisoflavone can be extracted from plants, such as yellow alfalfa and other plants contain higher content.
2. Chemical synthesis: 3 ',4',7-Trihydroxyisoflavone can also be synthesized by chemical reaction. The specific synthesis method is more complicated and often requires multi-step reaction.
With respect to safety information, no serious toxicities or side effects have been identified for 3 ',4', 7-trihydroxyisoflavone. However, like all chemical substances, it still needs to be handled carefully during use and strictly in accordance with safe operating procedures. Prior to use, it is advisable to conduct relevant toxicological studies to assess the potential toxicity risk. In addition, the correct concentration and dosage should be followed during use to reduce the risk of any potential adverse reactions.
OH OH
/
C=C
/
OH OH
The following are the properties of 3 ',4',7-Trihydroxyisoflavone:
1. Appearance: 3 ',4',7-Trihydroxyisoflavone is a yellow crystalline solid.
2. Solubility: It has low solubility in water and good solubility in organic solvents.
The main uses of 3 ',4',7-Trihydroxyisoflavone are as follows:
1. Antioxidant: It has strong antioxidant activity, can scavenge free radicals, protect cells from free radical damage.
2. Anti-inflammatory effect: 3 ',4',7-Trihydroxyisoflavone has inhibitory effect on inflammatory response and can be used to treat inflammation-related diseases.
3. Anticancer activity: Studies have shown that 3 ',4',7-Trihydroxyisoflavone has an inhibitory effect on certain cancer cells and may have anti-cancer potential.
The methods for preparing 3 ',4',7-Trihydroxyisoflavone mainly include natural extraction and chemical synthesis.
1. Natural extraction: 3 ',4',7-Trihydroxyisoflavone can be extracted from plants, such as yellow alfalfa and other plants contain higher content.
2. Chemical synthesis: 3 ',4',7-Trihydroxyisoflavone can also be synthesized by chemical reaction. The specific synthesis method is more complicated and often requires multi-step reaction.
With respect to safety information, no serious toxicities or side effects have been identified for 3 ',4', 7-trihydroxyisoflavone. However, like all chemical substances, it still needs to be handled carefully during use and strictly in accordance with safe operating procedures. Prior to use, it is advisable to conduct relevant toxicological studies to assess the potential toxicity risk. In addition, the correct concentration and dosage should be followed during use to reduce the risk of any potential adverse reactions.
Last Update：2024-04-10 22:29:15
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Product Name: 3,4,7-Trihydroxyisoflavone Visit Supplier Webpage Request for quotationCAS: 485-63-2
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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