6512-32-9

Basic information

• Product Name: 3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER
• Synonyms: METHYL 3,5-DIMETHOXYPHENYLACETATE;3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER;Benzeneacetic acid, 3,5-diMethoxy-, Methyl ester;Ethyl 3,5-diMethoxyphenylacetate;methyl 2-(3,5-dimethoxyphenyl)acetate
• CAS NO: 6512-32-9
• Molecular Formula: C₁₁H₁₄O₄
• Molecular Weight: 210.23
• Product Categories: Aromatic Esters
• Mol File: 6512-32-9.mol
• Article Data: 30

Chemical Properties

• Boiling Point: 94°C/0.04mmHg(lit.)
• Appearance: /
• Density: 1.105±0.06 g/cm3(Predicted)
• Refractive Index: 1.5200 to 1.5240
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly)
• CAS DataBase Reference: 3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER(6512-32-9)
• EPA Substance Registry System: 3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER(6512-32-9)

Safety Data

• Hazardous Substances Data: 6512-32-9(Hazardous Substances Data)

Usage

General Description

3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER, also known as methyldopa methyl ester, is a chemical compound that is commonly used in the synthesis of pharmaceutical drugs and organic compounds. It is a methyl ester derivative of 3,5-dimethoxyphenylacetic acid, a naturally occurring compound found in plant species. This chemical has been found to exhibit antihypertensive and antioxidant properties, making it a potential candidate for the development of new drugs for the treatment of hypertension and oxidative stress-related disorders. It is also used as a building block in the synthesis of various bioactive molecules and pharmaceutical intermediates. Additionally, it is commonly used as a reagent in organic chemistry for the preparation of other compounds.

Upstream product

• 4724-10-1 methyl 2-(3,5-dihydroxyphenyl)acetate 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 
• 4670-10-4 (3,5-dimethoxyphenyl)acetic acid 
• 74-88-4 methyl iodide 
• 1422166-78-6 3,5-dimethoxy-1-(2-methoxy-2-oxoethyl)cyclohexa-2,5-diene-1-carboxylic acid 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 
• 4670-09-1 2-(3,5-dihydroxyphenyl)acetic acid 
• 877-88-3 3,5-dimethoxybenzyl bromide 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 186581-53-3 diazomethane 
• 17213-57-9 3,5-dimethoxybenzoyl chloride 
• 13388-75-5 3,5-dimethoxyphenylacetonitrile 
• 1132-21-4 3,5-dimethoxybenzoic acid 

Downstream Products

• 7417-20-1 3,5-dimethoxyphenethyl alcohol 
• 602278-05-7 (2-formyl-3,5-dimethoxy-phenyl)-acetic acid methyl ester 
• 66761-59-9 2-Formyl-3,5-dimethoxyphenylacetic acid 
• 135387-90-5 (S)-4-Benzyl-3-[2-(3,5-dimethoxy-phenyl)-acetyl]-oxazolidin-2-one 
• 135387-93-8 (S)-3-[(S)-2-Azido-2-(3,5-dimethoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one 
• 103889-87-8 (S)-3,5-dimethoxyphenylglycine 
• 103889-85-6 (R)-3,5-dimethoxyphenylglycine 
• 81280-94-6 2-<3',5'-dimethoxy-2'-(1',7'-dioxo-octyl)benzyl>-4,5-diphenyloxazole 
• 81280-92-4 2-(3,5-dimethyloxyphenylmethyl)-4,5-diphenyloxazole 
• 81280-93-5 benzoin 3,5-dimethyloxyphenyl acetate 
• 81280-95-7 2-(3,5-dimethoxy-2-(7'-hydroxy-1'-oxooctyl)-phenylmethyl)-4,5-diphenyloxazole 
• 81280-96-8 N-Benzoyl-N-{2-[2-(7-hydroxy-octanoyl)-3,5-dimethoxy-phenyl]-acetyl}-benzamide 
• 17173-31-8 3,5-Dimethoxy-2-<7-hydroxy-octanoyl>-phenylessigsaeure-methylester 
• 710324-37-1 3-(2,4-Dichloro-pyrimidin-5-yl)-2-(3,5-dimethoxy-phenyl)-propionic acid methyl ester 

Relevant articles and documents

Xylochemical synthesis and biological evaluation of shancigusin c and bletistrin g

The biological activities of shancigusin C (1) and bletistrin G (2), natural products isolated from orchids, are reported along with their first total syntheses. The total synthesis of shancigusin C (1) was conducted by employing the Perkin reaction to forge the central stilbene core, whereas the synthesis of bletistrin G (2) was achieved by the Wittig olefination followed by several regiose-lective aromatic substitution reactions. Both syntheses were completed by applying only renewable starting materials according to the principles of xylochemistry. The cytotoxic properties of shancigusin C (1) and bletistrin G (2) against tumor cells suggest suitability as a starting point for further structural variation.

Identification of N,N-arylalkyl-picolinamide derivatives targeting the RNA-binding protein HuR, by combining biophysical fragment-screening and molecular hybridization

Hu proteins are members of the RNA-binding protein (RBP) family and play a pivotal role in the regulation of post-transcriptional processes. Through interaction with selected mRNAs, RBPs regulate their function and stability; as a consequence, RBP dysregu

Stereoselective total synthesis of (-)-curvularin

A concise total synthesis of (-)-Curvularin have been synthesized from commercially available (S)-(?)-propylene epoxide and (3,5-Dimethoxyphenyl)acetic acid. The key steps involved in the synthesis are Vilsmeier-Haack formylation, Grignard reaction, alkyl