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1,3-Benzenedicarboxylic acid, 4,6-dimethoxy, dimethyl ester is a chemical compound with the molecular formula C12H14O8. It is an organic ester derived from 1,3-benzenedicarboxylic acid, also known as isophthalic acid, with two methoxy groups attached at the 4 and 6 positions and two methyl ester groups. 1,3-Benzenedicarboxylic acid, 4,6-dimethoxy-, dimethyl ester is characterized by its aromatic structure, which consists of a benzene ring with two carboxylic acid groups at the 1 and 3 positions. The presence of the methoxy groups and methyl esters contributes to its unique chemical properties, making it a versatile compound with potential applications in various industries, such as pharmaceuticals, polymers, and dyes.

14965-05-0

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14965-05-0 Usage

Chemical structure

1,3-Benzenedicarboxylic acid, 4,6-dimethoxy-, dimethyl ester

Physical state

White, crystalline solid

Usage

a. Production of polyester resins
b. Manufacturing of packaging materials, textiles, and electronics
c. Intermediate in the production of polyethylene terephthalate (PET) resin
d. Production of plastic bottles and containers
e. Solvent
f. Pharmaceutical industry

Health risks

a. Potential for skin irritation
b. Potential for eye irritation
c. Potential for respiratory system irritation
d. Proper handling required to minimize exposure

Environmental impact

May pose environmental concerns if not disposed of or managed properly

Check Digit Verification of cas no

The CAS Registry Mumber 14965-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,6 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14965-05:
(7*1)+(6*4)+(5*9)+(4*6)+(3*5)+(2*0)+(1*5)=120
120 % 10 = 0
So 14965-05-0 is a valid CAS Registry Number.

14965-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dimethoxy-isophtalic acid dimethyl ester

1.2 Other means of identification

Product number -
Other names 4,6-dimethoxyisophthalic acid dimethyl 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:14965-05-0 SDS

14965-05-0Downstream Products

14965-05-0Relevant academic research and scientific papers

Aromatic amides metal ligand capable of forming intramolecular hydrogen bond and preparation method and application thereof

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Paragraph 0048; 0049, (2019/02/19)

The invention provides an aromatic amides metal ligand capable of forming an intramolecular hydrogen bond and a preparation method and application thereof, and belongs to the technical field of coordination polymer materials. In allusion to a problem in t

Synthesis of crescent aromatic oligoamides

Yuan, Lihua,Sanford, Adam R.,Feng, Wen,Zhang, Aimin,Zhu, Jin,Zeng, Huaqiang,Yamato, Kazuhiro,Li, Minfeng,Ferguson, Joseph S.,Gong, Bing

, p. 10660 - 10669 (2007/10/03)

This article describes the synthetic procedures for the preparation of crescent (and helical) aromatic oligoamides developed in recent years in our laboratory. The large-scale preparation of a variety of monomers derived from various tetrasubstituted benzenes is presented. Three different strategies for constructing various oligomers consisting of meta- and meta/para-linked benzene residues are discussed. Factors affecting coupling efficiency and yields are analyzed. The developed synthetic methods have provided the basis for the preparation of longer oligomers and for the development of solid-phase synthesis.

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