Methyl 2-(m-tolyl)acetate
98%
- Product Code: 83306
Alias:
Methyl 3-methylphenylacetate
CAS:
53088-69-0
Molecular Weight: | 164.20 g./mol | Molecular Formula: | C₁₀H₁₂O₂ |
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EC Number: | MDL Number: | MFCD00968468 | |
Melting Point: | Boiling Point: | 226.9°C at 760 mmHg | |
Density: | Storage Condition: | room temperature |
Product Description:
Methyl 2-(m-tolyl)acetate finds its primary application in the field of organic synthesis, where it serves as a versatile intermediate. It is commonly used in the production of fine chemicals and pharmaceuticals, particularly in the synthesis of compounds with aromatic structures. Its ester functional group makes it a valuable building block for creating more complex molecules through reactions such as hydrolysis, transesterification, or reduction. Additionally, it is employed in the development of fragrances and flavoring agents due to its aromatic properties, contributing to the creation of pleasant scents and tastes in consumer products. Its role in research and development also extends to the study of chemical reactions and the exploration of new synthetic pathways.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,107.00 |
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1.000 | 10-20 days | ฿2,178.00 |
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5.000 | 10-20 days | ฿4,770.00 |
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Methyl 2-(m-tolyl)acetate
Methyl 2-(m-tolyl)acetate finds its primary application in the field of organic synthesis, where it serves as a versatile intermediate. It is commonly used in the production of fine chemicals and pharmaceuticals, particularly in the synthesis of compounds with aromatic structures. Its ester functional group makes it a valuable building block for creating more complex molecules through reactions such as hydrolysis, transesterification, or reduction. Additionally, it is employed in the development of fragrances and flavoring agents due to its aromatic properties, contributing to the creation of pleasant scents and tastes in consumer products. Its role in research and development also extends to the study of chemical reactions and the exploration of new synthetic pathways.
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