1,3-Bis(4-methoxyphenyl)-1,3-propanedione
98%
- Product Code: 68012
CAS:
18362-51-1
Molecular Weight: | 284.31 g./mol | Molecular Formula: | CH₃OC₆H₄CO₂CH₂ |
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EC Number: | 242-233-2 | MDL Number: | MFCD00025817 |
Melting Point: | 108-115 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the preparation of more complex molecules. Its structure, featuring two methoxyphenyl groups, makes it particularly useful in the development of pharmaceuticals, especially in the synthesis of compounds with potential therapeutic properties. Additionally, it is employed in the creation of organic electronic materials, where its conjugated system can contribute to the desired electronic properties. In research, it is often used to study reaction mechanisms and to develop new synthetic methodologies, particularly those involving diketone chemistry.
Product Specification:
Test | Specification |
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Melting point | 115-118 |
PurityGC | 98-100 |
WATER BY KARL FISCHER | 0-1 |
APPEARANCE | Yellow powder or crystals |
INFRARED SPECTRUM | Conforms to Structure |
NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿2,952.00 |
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5.000 | 10-20 days | ฿8,874.00 |
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25.000 | 10-20 days | ฿30,276.00 |
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1,3-Bis(4-methoxyphenyl)-1,3-propanedione
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the preparation of more complex molecules. Its structure, featuring two methoxyphenyl groups, makes it particularly useful in the development of pharmaceuticals, especially in the synthesis of compounds with potential therapeutic properties. Additionally, it is employed in the creation of organic electronic materials, where its conjugated system can contribute to the desired electronic properties. In research, it is often used to study reaction mechanisms and to develop new synthetic methodologies, particularly those involving diketone chemistry.
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