Thiencarbazone-methyl Inter
81528-48-5
Physical Form: Solid
Purity: 98%
Storage Temp.: Keep in dark place,Inert atmosphere,2-8C
Availability: | |
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Product Description
We are a agrochem intermediates manufacturer of 81528-48-5 Methyl 4-aMino-5-Methylthiophene-3-carboxylate.
Its CAS No. is 81528-48-5.
Our agrochem Intermediates can be used in a variety of APIs such as saflufenacil inters,thiencarbazonemethyl inters,pyroxsulam inters,flubendiamide inters,etc.
Product Category | Thiencarbazone-methyl Inter |
CAS NO | 81528-48-5 |
Product Specifications | Physical Form: Solid Purity: 98% Storage Temp.: Keep in dark place,Inert atmosphere,2-8C |
81528-48-5 Methyl 4-aMino-5-Methylthiophene-3-carboxylate.pdf
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81528-48-5 Methyl 4-aMino-5-Methylthiophene-3-carboxylate is produced by EASTFINE , and we are in charge of overseas selling . Not just trading compamy .
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yes , you can have 1 81528-48-5 Methyl 4-aMino-5-Methylthiophene-3-carboxylate sample for starting the business , but it is not free
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This compound is often used as an intermediate in the synthesis of pharmaceuticals or biologically active molecules. It might also be useful in the development of compounds for agrochemical applications. The presence of both an amino group and a carboxylate group gives it versatility for further modifications.
The thiophene ring provides aromaticity and stability, while the amino group and methyl ester allow for further chemical reactions, such as amination or ester hydrolysis. The methyl group at the 5-position also influences its reactivity and solubility in organic solvents.
As with many organic chemicals, the toxicity of Methyl 4-amino-5-methylthiophene-3-carboxylate should be assessed before handling. However, for many aromatic amines and thiophene derivatives, handling precautions such as the use of gloves, goggles, and ventilation are advised to minimize exposure. It's essential to consult safety data sheets (SDS) for specific toxicity information.
The methyl ester group (-COOCH₃) is a common functional group that can be easily hydrolyzed (split) into a carboxylic acid and methanol, or it can undergo further chemical reactions. This makes it a useful group for modifying the compound in the synthesis of more complex molecules.
Methyl 4-amino-5-methylthiophene-3-carboxylate can be purchased from chemical supply companies that provide specialized reagents for organic synthesis. It might also be available from research-grade chemical suppliers for use in academic or industrial laboratories.
As an intermediate, this compound could be part of the development of molecules with potential pharmacological activity, especially in the areas of anti-inflammatory, antimicrobial, or antioxidant research. Thiophene derivatives are known to possess a range of biological activities and may be of interest in drug design.
Yes, due to its reactive functional groups, Methyl 4-amino-5-methylthiophene-3-carboxylate could be used in the synthesis of more complex molecules, such as other thiophene-based compounds or heterocyclic pharmaceuticals. Researchers may use this compound to modify the aromatic system or to attach additional functional groups for further testing.
Like most organic chemicals, it should be stored in a cool, dry place and kept in a tightly sealed container to avoid moisture or contamination. Specific storage instructions would be detailed in the Safety Data Sheet (SDS) for the compound.
The environmental impact of Methyl 4-amino-5-methylthiophene-3-carboxylate would need to be assessed through ecological studies. However, as it is an organic chemical, it should be disposed of in accordance with local hazardous waste regulations to avoid contamination.