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DIMETHYL 3-BROMOPHTHALATE, with the molecular formula C10H9BrO4, is a white crystalline powder that serves as a versatile intermediate in the synthesis of various organic compounds. Its reactivity and versatility in organic synthesis make it a valuable component in the production of pharmaceuticals, agrochemicals, and for chemical research purposes. Due to its potential to cause irritation to the skin, eyes, and respiratory system, it is crucial to handle and store DIMETHYL 3-BROMOPHTHALATE with appropriate safety measures, including keeping it in a cool, dry, and well-ventilated environment away from ignition sources and incompatible materials.

58749-33-0

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58749-33-0 Usage

Uses

Used in Pharmaceutical Industry:
DIMETHYL 3-BROMOPHTHALATE is used as a key intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and medicines.
Used in Agrochemical Industry:
In the agrochemical sector, DIMETHYL 3-BROMOPHTHALATE is utilized as an intermediate for the production of agrochemicals, aiding in the creation of substances that protect crops and enhance agricultural productivity.
Used in Chemical Research:
DIMETHYL 3-BROMOPHTHALATE is employed as a research chemical, facilitating the exploration of new chemical reactions and the development of innovative organic synthesis methods.

Check Digit Verification of cas no

The CAS Registry Mumber 58749-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,4 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58749-33:
(7*5)+(6*8)+(5*7)+(4*4)+(3*9)+(2*3)+(1*3)=170
170 % 10 = 0
So 58749-33-0 is a valid CAS Registry Number.

58749-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 3-bromobenzene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3-Brom-phthalsaeure-dimethylester

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:58749-33-0 SDS

58749-33-0Relevant academic research and scientific papers

SUBSTITUTED ISOINDOLINONES

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Paragraph 0146, (2020/06/05)

Substituted isoindolinones of Formula (I), methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat or ameliorate diseases, disorders, or conditions associated with protein malfunction, such as cancer, are provided.

Conception of myeloperoxidase inhibitors derived from flufenamic acid by computational docking and structure modification

Van Antwerpen, Pierre,Prevost, Martine,Zouaoui-Boudjeltia, Karim,Babar, Sajida,Legssyer,Moreau, Patrick,Moguilevsky, Nicole,Vanhaeverbeek, Michel,Ducobu, Jean,Neve, Jean,Dufrasne, Francois

, p. 1702 - 1720 (2008/09/20)

The development of myeloperoxidase (MPO) inhibitors has been conducted using flufenamic acid as a lead compound. Computational docking of the drug and its analogs in the MPO active site was first attempted. Several molecules were then synthesized and assessed using three procedures for the measurement of their inhibiting activity: (i) the taurine assay, (ii) the accumulation of compound II, and (iii) the LDL oxidation by ELISA. Most of the synthesized molecules had an activity in the same range as flufenamic acid but none of them were able to inhibit the MPO-dependent LDL oxidation. The experiments however gave some useful indications for a rational conception of MPO inhibitors.

Isoindole-imide compounds and compositions comprising and methods of using the same

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Page/Page column 70, (2010/11/26)

This invention relates to isoindole-imide compounds, and pharmaceutically acceptable salts, solvates, stereoisomers, and prodrugs thereof. Methods of use, and pharmaceutical compositions of these compounds are disclosed.

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