2800-99-9

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

1,4-Benzenedimethanol, 2,5-dichlorois derived from benzenedimethanol, which is a colorless, viscous liquid with a mild, pleasant odor.

Explanation

The compound is in a liquid state at room temperature.

Explanation

The compound is colorless, meaning it does not have any visible color.

Explanation

The compound has a mild and pleasant odor, making it less offensive to the senses.

Explanation

The presence of chlorine atoms at these specific positions on the benzene ring contributes to the compound's properties and applications.

Explanation

The compound's structure makes it a useful starting material for creating a range of other chemicals and materials.

Explanation

The compound has antimicrobial properties, which means it can inhibit the growth of microorganisms.

Explanation

Due to its antimicrobial properties, the compound is often used in the formulation of disinfectants and sanitizers to help kill or inhibit the growth of harmful microorganisms.

Explanation

It is important to handle 1,4-Benzenedimethanol, 2,5-dichloro- with care, as it can cause irritation upon contact with the skin, eyes, or if inhaled. Proper safety measures should be taken when working with this chemical.

Derivative of benzenedimethanol

Yes

Physical state

Liquid

Color

Colorless

Odor

Mild, pleasant

Chlorine atoms

At the 2 and 5 positions of the benzene ring

Use as a building block

For the synthesis of various polymers, resins, and specialty chemicals

Antimicrobial properties

Yes

Application in disinfectants and sanitizers

Commonly used as an ingredient

Safety precautions

Can be irritating to skin, eyes, and respiratory system

Upstream product

• 107-31-3 Methyl formate 
• 50987-90-1 1,4-bis(chloromethyl)-2,5-dichlorobenzene 
• 56-93-9 benzyltrimethylammonium chloride 
• 130208-54-7 ((1S,4S)-2,5-Dichloro-4-hydroxymethyl-bicyclo[2.2.0]hexa-2,5-dien-1-yl)-methanol 
• 13799-90-1 2,5-dichloroterephthalic acid 

Downstream Products

• 21004-03-5 2,5-dichloro-7,7,8,8-tetracyano-p-quinodimethane 
• 21004-02-4 Dimethyl α,α,α',α'-Tetracyano-2,5-dichlor-p-phenylendiacetat 
• 56403-43-1 1,4-Bis-(cyanomethyl)-2,5-dichlorbenzol 
• 50987-90-1 1,4-bis(chloromethyl)-2,5-dichlorobenzene 

Relevant academic research and scientific papers

Convenient Synthesis of Some Functionalized Dewar Benzenes and Effect of Chlorine Substitution on the Rates of Their Aromatization

1,4-Bis(hydroxymethyl) Dewar benzenes were prepared in five steps from dimethyl acetylenedicarboxylate in ca. 10percent overall yield and rates of their aromatization were measured: dichloro substitution at both the 2,5- and 2,6-positions led to substantial deceleration of the isomerization.

Process for preparing benzylalcohols

There is described an essentially two step process for the preparation of benzylalcohols including those benzylalcohols having substituents on the benzyene ring by reaction of a substituted or unsubstituted benzyl halide with a formate typically an alkali or alkaline earth metal formate to form the corresponding substituted or unsubstituted benzyl formate. In the second step of the process the benzyl formate is contacted with an alcohol whereby the same is converted into the desired benzylalcohol. Both steps can be performed employing catalysts. Described in the specification is the realization of the desired product in exceptionally high yields in a short period of time whereby the process is characterized by high space-time yields.