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3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER, also known as methyldopa methyl ester, is a chemical compound that serves as a methyl ester derivative of 3,5-dimethoxyphenylacetic acid, a naturally occurring substance in certain plant species. This versatile chemical is recognized for its antihypertensive and antioxidant properties, positioning it as a promising candidate for the development of pharmaceuticals targeting hypertension and oxidative stress-related conditions. Furthermore, it plays a crucial role as a building block in the synthesis of bioactive molecules and pharmaceutical intermediates, and is utilized as a reagent in organic chemistry for the preparation of other compounds.

6512-32-9

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6512-32-9 Usage

Uses

Used in Pharmaceutical Industry:
3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER is used as a key intermediate for the synthesis of pharmaceutical drugs, leveraging its antihypertensive and antioxidant properties to develop new treatments for hypertension and oxidative stress-related disorders.
Used in Organic Chemistry:
3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER is used as a reagent for the preparation of other organic compounds, contributing to the synthesis of a variety of bioactive molecules and pharmaceutical intermediates, thereby enhancing the scope of chemical research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 6512-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6512-32:
(6*6)+(5*5)+(4*1)+(3*2)+(2*3)+(1*2)=79
79 % 10 = 9
So 6512-32-9 is a valid CAS Registry Number.

6512-32-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-DIMETHOXYPHENYLACETIC ACID METHYL ESTER

1.2 Other means of identification

Product number -
Other names Benzeneacetic acid,3,5-diMethoxy-,Methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6512-32-9 SDS

6512-32-9Relevant academic research and scientific papers

Xylochemical synthesis and biological evaluation of shancigusin c and bletistrin g

Efferth, Thomas,Geske, Leander,Kauhl, Ulrich,Opatz, Till,Saeed, Mohamed E. M.,Schüffler, Anja,Thines, Eckhard

supporting information, (2021/06/16)

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.

Synthesis of (+)-xestodecalactone A

Mura Reddy, Gudisela,Prasad, K. R. S.,Reddy, G. Nagendra,Sridhar, Gattu

supporting information, (2021/06/27)

The total synthesis of Benzannulated macrolide, (+)-Xestodecalactone A was accomplished starting from commercially available enantiomerically pure propylene oxide and 3,5-dihydroxyphenylacetic acid using Grignard reaction, alkylation of 1,3-dithiane and Y

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

Della Volpe,Linciano,Listro,Tumminelli,Amadio,Bonomo,Elgaher,Adam,Hirsch,Boeckler,Vasile,Rossi,Collina

, (2021/09/06)

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

Concise Total Synthesis of Curvulone B

Banoth, Shivalal,Choudhury, Utkal Mani,Marumudi, Kanakaraju,Kunwar, Ajit C.,Mohapatra, Debendra K.

supporting information, p. 685 - 688 (2020/12/07)

A concise and convergent stereoselective synthesis of curvulone B is described. The synthesis utilized a tandem isomerization followed by C-O and C-C bond-forming reactions following Mukaiyama-Type aldol conditions for the construction of the trans-2,6-di

Stereoselective total synthesis of (-)-curvularin

Jayaprakash, H. V.,Radha Krishna, Muniganti,Sridhar, Gattu,Syed, Tasqeeruddin

supporting information, (2021/12/22)

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

Blue Light-Promoted N?H Insertion of Carbazoles, Pyrazoles and 1,2,3-Triazoles into Aryldiazoacetates

Stivanin, Mateus L.,Fernandes, Alessandra A. G.,da Silva, Amanda F.,Okada, Celso Y.,Jurberg, Igor D.

supporting information, p. 1106 - 1111 (2020/01/25)

Blue light irradiation of aryldiazoacetates leads to the formation of free carbenes, which can react with carbazoles, pyrazoles and 1,2,3-triazoles to afford the corresponding N?H inserted products. These reactions are performed under air and at room temperature, allowing the mild preparation of a variety of motifs found in biologically relevant targets. (Figure presented.).

Room Temperature Coupling of Aryldiazoacetates with Boronic Acids Enhanced by Blue Light Irradiation

da Silva, Amanda F.,Afonso, Marco A. S.,Cormanich, Rodrigo A.,Jurberg, Igor D.

supporting information, p. 5648 - 5653 (2020/04/22)

A visible-light-promoted photochemical protocol is reported for the coupling of aryldiazoacetates with boronic acids. This photochemical reaction shows great enhancement compared to the same protocol performed in the absence of light. Except for a few cases, the room temperature coupling in the dark (thermal process) generally does not work. When it does, it is likely to also involve free carbenes as key intermediates. Alternatively, photochemical reactions show a broad scope, can be performed under air and tolerate a wide variety of functional groups. Reaction-evolution monitoring, DFT calculations and control experiments have been used to evaluate the main aspects of this intricate mechanistic scenario. Biologically active molecules Adiphenine, Benactyzine and Aprophen have been prepared as examples of synthetic applications.

A Unified Synthetic Approach to Optically Pure Curvularin-Type Metabolites

Allu, Srinivasa Rao,Banne, Sreenivas,Jiang, Jia,Qi, Na,Guo, Jian,He, Yun

, p. 7227 - 7237 (2019/06/07)

A unified and concise approach to the synthesis of nine curvularin-type metabolites and two analogues has been developed with few steps and high yields. Among them, sumalactones A-D were synthesized for the first time. The key steps in this approach inclu

PROCESSES FOR PREPARING AN FGFR INHIBITOR

-

Page/Page column 27-28, (2017/03/17)

Disclosed herein are processes for preparing 8-(3-(4-acryloylpiperazin-l-yl)propyl)-6-(2,6-dichloro-3,5-dimethoxyphenyl)-2- (methylamino)pyrido[2,3-d]pyrimidin-7(8H)-one and FGFR inhibitor, as well as polymorphs and/or salt forms thereof.

Inhibitors of the fibroblast growth factor receptor

-

Page/Page column 49, (2017/08/01)

Described herein are inhibitors of FGFR-4, pharmaceutical compositions including such compounds, and methods of using such compounds and compositions to inhibit the activity of FGFR-4.

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