Ethyl 4-amino-3-methoxybenzoate
97%
- Product Code: 119008
CAS:
73368-41-9
Molecular Weight: | 195.22 g./mol | Molecular Formula: | C₁₀H₁₃NO₃ |
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EC Number: | MDL Number: | MFCD14543019 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of drugs targeting neurological and cardiovascular conditions. Its structure makes it a valuable precursor in the production of active pharmaceutical ingredients (APIs) that exhibit therapeutic effects. Additionally, it is employed in organic synthesis for creating complex molecules used in medicinal chemistry research. The compound also finds application in the production of dyes and pigments, where its chemical properties contribute to the stability and color intensity of the final products. In research laboratories, it is often used as a reagent in various chemical reactions to study reaction mechanisms and develop new synthetic pathways.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿270.00 |
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0.250 | 10-20 days | ฿351.00 |
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1.000 | 10-20 days | ฿873.00 |
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5.000 | 10-20 days | ฿2,205.00 |
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Ethyl 4-amino-3-methoxybenzoate
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of drugs targeting neurological and cardiovascular conditions. Its structure makes it a valuable precursor in the production of active pharmaceutical ingredients (APIs) that exhibit therapeutic effects. Additionally, it is employed in organic synthesis for creating complex molecules used in medicinal chemistry research. The compound also finds application in the production of dyes and pigments, where its chemical properties contribute to the stability and color intensity of the final products. In research laboratories, it is often used as a reagent in various chemical reactions to study reaction mechanisms and develop new synthetic pathways.
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