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1,3-Dioxolane, 2,2'-(1,4-butanediyl)bis-, also known as 2,2'-(1,4-butanediyl)bis-1,3-dioxolane or simply bis(1,3-dioxolane), is a cyclic ether compound with the molecular formula C8H14O4. It consists of two 1,3-dioxolane rings connected by a butane chain, forming a symmetrical structure. This organic compound is characterized by its low toxicity, high solubility in water, and excellent thermal stability. It is commonly used as a solvent, stabilizer, and intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals. Due to its unique properties, bis(1,3-dioxolane) plays a significant role in various industrial applications, making it an important chemical in the field of organic chemistry.

6543-02-8

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6543-02-8 Usage

Explanation

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

Explanation

The chemical structure describes the arrangement of atoms and the type of bonds between them in the compound.

Explanation

A solvent is a substance that dissolves a solute to form a solution, which can be used in various chemical reactions and processes.

Explanation

A precursor is a substance that can be chemically converted into another compound through a series of reactions.

Explanation

A reagent is a substance or compound used to initiate a chemical reaction, often serving as a catalyst or reactant.

Explanation

A stabilizer is a substance added to a material to improve its stability, preventing degradation or deterioration over time.

Explanation

The compound has been found to be harmful to aquatic life, which can have negative consequences for the environment.

Explanation

The compound's presence in the environment can lead to negative, lasting effects on ecosystems and natural habitats.

Explanation

To minimize the potential harm to the environment and human health, it is essential to follow appropriate safety measures when using, storing, and disposing of the compound.

Chemical structure

Cyclic ether with two dioxolane rings bridged by a 1,4-butanediyl group

Solvent

Commonly used as a solvent

Precursor

Used as a precursor for the synthesis of other organic compounds

Reagent

Used as a reagent in organic synthesis

Stabilizer

Used as a stabilizer in the production of polymers

Toxicity

Toxic to aquatic organisms

Environmental impact

May cause long-term adverse effects in the environment

Handling and disposal

Proper handling and disposal procedures should be followed

Check Digit Verification of cas no

The CAS Registry Mumber 6543-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6543-02:
(6*6)+(5*5)+(4*4)+(3*3)+(2*0)+(1*2)=88
88 % 10 = 8
So 6543-02-8 is a valid CAS Registry Number.

6543-02-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-butane-1,4-diyl-bis-[1,3]dioxolane

1.2 Other means of identification

Product number -
Other names 1,4-Di-[1,3]dioxolan-2-yl-butan

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:6543-02-8 SDS

6543-02-8Relevant academic research and scientific papers

Nickel-catalyzed cross-coupling of alkyl zinc halides for the formation of C(sp2)-C(sp3) bonds: Scope and mechanism

Phapale, Vilas B.,Guisan-Ceinos, Manuel,Bunuel, Elena,Cardenas, Diego J.

supporting information; experimental part, p. 12681 - 12688 (2010/06/12)

Optimal conditions for a general Ni-catalysed Negishi cross-coupling of alkyl zinc halides with aryl, heteroaryl and alkenyl halides have been determined. These conditions allow the reaction to take place smoothly, with low catalyst loading, and in the pr

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