951-82-6 3,4,5-Trimethoxyphenylacetic acid

951-82-6 3,4,5-Trimethoxyphenylacetic acid Introduction

We are a pharmaceutical intermediate manufacturer of 3,4,5-Trimethoxyphenylacetic acid.

Its CAS No. is 951-82-6.

3,4,5-Trimethoxyphenylacetic acid is an organic compound with the molecular formula C10H12O5. It is a phenylacetic acid derivative, where a phenyl group (a benzene ring) is attached to an acetic acid functional group (-COOH), and three methoxy groups (-OCH3) are attached at the 3, 4, and 5 positions on the benzene ring.

Our pharmaceutical intermediates can be used in a variety of APIs such as Articaine, Pyrantel, Bicalutamide, Apalutamide, etc.

951-82-6 3,4,5-Trimethoxyphenylacetic acid Specifications

951-82-6 3,4,5-Trimethoxyphenylacetic acid PDF

951-82-6 3,4,5-TRIMETHOXYPHENYLACETIC ACID.pdf

951-82-6 3,4,5-Trimethoxyphenylacetic acid Factory display

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951-82-6 3,4,5-Trimethoxyphenylacetic acid Certification

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951-82-6 3,4,5-Trimethoxyphenylacetic acid FAQ

1. Manufacturer or trading company for 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

3,4,5-Trimethoxyphenylacetic acid is produced by EASTFINE , and we are in charge of  overseas selling . Not just trading company .

2. 951-82-6 3,4,5-Trimethoxyphenylacetic acid supplier and factories or wholesale locates in such countries like?

China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.

3. Can I get a sample for trying 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

Yes , you can have 3,4,5-Trimethoxyphenylacetic acid sample for starting the business , but it is not free

4. What the MOQ of 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

Please contact our sales team for more details.

5. What is 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

3,4,5-Trimethoxyphenylacetic acid is an organic compound consisting of a phenylacetic acid structure, with three methoxy groups (-OCH3) attached to the 3, 4, and 5 positions on the phenyl ring. Its molecular formula is C10H12O5.

6. What are the applications of 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

· Organic synthesis: It can be used as an intermediate in the synthesis of more complex molecules, particularly in the production of pharmaceuticals and agrochemicals.

· Medicinal chemistry: The compound is of interest for research due to its structure, which may provide bioactivity through its interaction with specific biological targets.

· Natural product synthesis: The compound is related to several natural products and may serve as a precursor or building block for bioactive compounds.

7. What is the structure of 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

The structure consists of a phenylacetic acid backbone (a benzene ring attached to an acetic acid group) with three methoxy groups (-OCH3) attached at the 3, 4, and 5 positions of the aromatic ring. These methoxy groups contribute electron-donating properties, which can influence the molecule's reactivity.

8. How is 951-82-6 3,4,5-Trimethoxyphenylacetic acid synthesized?

3,4,5-Trimethoxyphenylacetic acid can be synthesized through several methods, typically involving the following steps:

· Electrophilic aromatic substitution: Methoxy groups are introduced onto a phenylacetic acid core by reacting the starting material with methylating reagents (such as methyl iodide) in the presence of a catalyst (like potassium carbonate or sodium hydroxide).

· Selective methylation: Precise control of reaction conditions ensures that the methoxy groups are installed at the 3, 4, and 5 positions on the phenyl ring.

9. What are the physical properties of 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

· Appearance: The compound typically appears as a white solid.

· Solubility: It is moderately soluble in organic solvents like ethanol or acetone but may have low solubility in water due to the presence of the methoxy groups and the carboxylic acid group.

10. What is the role of the methoxy groups in 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

The methoxy groups (-OCH3) at the 3, 4, and 5 positions of the phenyl ring are electron-donating groups. This affects the compound's chemical reactivity, particularly in electrophilic substitution reactions. The methoxy groups also contribute to the compound's stability and could influence its interaction with biological targets in medicinal chemistry.

11. Is 951-82-6 3,4,5-Trimethoxyphenylacetic acid used in pharmaceuticals?

While 3,4,5-trimethoxyphenylacetic acid itself may not be a widely used pharmaceutical agent, it is an important intermediate in the synthesis of bioactive molecules. The presence of methoxy groups and the phenylacetic acid core structure make it a useful precursor in designing molecules with potential pharmacological activity.

12. What are the potential risks of handling 951-82-6 3,4,5-Trimethoxyphenylacetic acid?

· Toxicity: There is limited specific information on the toxicity of 3,4,5-trimethoxyphenylacetic acid, but it should be handled with care in a laboratory setting. As a general rule, chemicals with carboxylic acid groups should be handled with caution, as they can be irritating to the skin, eyes, and mucous membranes.

· Safety precautions: Use personal protective equipment (PPE) such as gloves, goggles, and lab coats, and work in a well-ventilated area or fume hood.

13. Can 951-82-6 3,4,5-Trimethoxyphenylacetic acid undergo further chemical reactions?

Yes, 3,4,5-Trimethoxyphenylacetic acid can undergo various chemical reactions, such as:

· Esterification: Reaction with alcohols can form esters, which are commonly used in organic synthesis.

· Reduction: The carboxylic acid group could be reduced to an aldehyde or alcohol.

· Nucleophilic substitution: The methoxy groups might be involved in reactions with electrophiles or other reactive species.

14. How does the presence of methoxy groups affect the molecule's reactivity?

The methoxy groups are electron-donating through resonance and inductive effects, which generally make the aromatic ring more reactive towards electrophilic substitution reactions. This can influence the molecule’s reactivity in various organic reactions.