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1,2-Benzenedicarboxylic acid, 4-chloro-, 1,2-dimethyl ester, also known as dimethyl terephthalate (DMT), is a colorless to pale yellow liquid with a faint aromatic odor. It is a chemical compound that serves as an important intermediate in the production of polyethylene terephthalate (PET) resin. This flammable substance can react violently with strong oxidizing agents, necessitating careful handling and storage to prevent potential hazards to human health and the environment.

58138-38-8

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58138-38-8 Usage

Uses

Used in Plastic Industry:
1,2-Benzenedicarboxylic acid, 4-chloro-, 1,2-dimethyl ester is used as a plasticizer for the production of polyethylene terephthalate (PET) resin. This resin is widely utilized in the manufacturing of plastic bottles and containers, making it a crucial component in the creation of various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 58138-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,3 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58138-38:
(7*5)+(6*8)+(5*1)+(4*3)+(3*8)+(2*3)+(1*8)=138
138 % 10 = 8
So 58138-38-8 is a valid CAS Registry Number.

58138-38-8SDS

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 dimethyl 4-chlorobenzene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 4-Chlor-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:58138-38-8 SDS

58138-38-8Relevant academic research and scientific papers

Preparation method for biphenyltetracarboxylic dianhydride mixture

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Paragraph 0030; 0031, (2016/10/09)

The invention relates to a preparation method for a biphenyltetracarboxylic dianhydride mixture. The preparation method comprises the following steps: with phthalic acid as a starting raw material, carrying out an electrophilic substitution reaction so as to produce a phthalic acid derivative; then subjecting the derivative to esterification so as to produce phthalate; further catalyzing phthalate and carrying out a coupling reaction so as to produce a biphenyl tetraformate mixture; and finally, successively carrying out saponification and acidification so as to produce the product biphenyltetracarboxylic dianhydride mixture. The method provided by the invention uses cheap and easily phthalic acid as the starting raw material and is a novel low-cost easily-operatable environment-friendly production method for biphenyltetracarboxylic dianhydride; moreover, isomeric compounds of all the biphenyltetracarboxylic dianhydride are synthesized at one time in the invention, so efficiency is improved and the cost is reduced.

Azabicyclic compounds for the treatment of disease

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Page 42, (2010/02/06)

The invention provides compounds of Formula I: wherein Azabicyclo is W is a six-membered heterocyclic ring system having 1-2 nitrogen atoms or a 10-membered bicyclic-six-six-fused-ring system having up to two nitrogen atoms within either or both rings, provided that no nitrogen is at a bridge of the bicyclic-six-six-fused-ring system, and further having 1-2 substitutents independently selected from R3. These compounds may be in the form of pharmaceutical salts or compositions, may be in pure enantiomeric form or racemic mixtures, and are useful in pharmaceuticals to treat diseases or conditions in which α7 is known to be involved.

The Diels-Alder approach to musk odor type arenes

Shi,Cottens,Shiba,Schlosser

, p. 10569 - 10574 (2007/10/02)

The readily accessible 2-halogeno-1-trimethylsilyloxy-1,3-butadienes react smoothly with dimethyl acetylenedicarboxylate to afford 4-halophthalic esters. One of these cycloadducts was subsequently converted into heterocyclic analogues of phantolide like musk fragrances.

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