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944-26-3

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944-26-3 Usage

Description

2,2'-Ethylenebis(2-methyl-1,3-dioxolane), with the chemical abstracts service number 944-26-3, is an organic compound that plays a significant role in various chemical processes and applications. It is characterized by its unique structure, which consists of two methyl-1,3-dioxolane rings connected by an ethylene bridge. This structure endows it with specific properties that make it valuable in the field of organic synthesis.

Uses

Used in Organic Synthesis:
2,2'-Ethylenebis(2-methyl-1,3-dioxolane) is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the synthesis of complex molecules and contributing to the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2'-Ethylenebis(2-methyl-1,3-dioxolane) serves as a key building block in the synthesis of certain drugs. Its ability to form stable intermediates and participate in various types of chemical reactions makes it an essential component in the development of new medications and therapies.
Used in Agrochemical Industry:
2,2'-Ethylenebis(2-methyl-1,3-dioxolane) is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its versatility in organic synthesis allows for the creation of novel compounds with improved efficacy and reduced environmental impact.
Used in Specialty Chemicals:
In the specialty chemicals sector, 2,2'-Ethylenebis(2-methyl-1,3-dioxolane) is employed in the production of various high-value compounds. Its unique properties enable it to be used in the synthesis of materials with specific applications, such as advanced polymers, surfactants, and other performance chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 944-26-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 944-26:
(5*9)+(4*4)+(3*4)+(2*2)+(1*6)=83
83 % 10 = 3
So 944-26-3 is a valid CAS Registry Number.

944-26-3SDS

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 2-methyl-2-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 2,cyclic bis(1,2-ethanediyl acetal)

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:944-26-3 SDS

944-26-3Downstream Products

944-26-3Relevant articles and documents

Preparation et oxydation anodique d'acides β-cetaliques. Application a la synthese de γ-bisdioxolannes symetriques et des γ-dicetones derivees.

Einhorn, Jacques,Soulier, Jean-Louis,Bacquet Cathy,Lelandais Daniel

, p. 584 - 587 (2007/10/02)

Anoxic oxidation of carboxylic acids with β-dioxolane substituents leads to good yields of symmetrical γ-bisdioxolanes.Hydrolysis of these compounds easily provides the corresponding γ-diketones.The synthesis of the starting acids is described.

SYNTHESE ELECTROCHIMIQUE DE METHOXY-2 DIOXA-1,4 CYCLANES PAR OXYDATION ANODIQUE DE CETALS CYCLIQUES DE β-CETO-CARBOXYLATES

Lelandais, Daniel,Bacquet, Cathy,Einhorn, Jacques

, p. 3131 - 3134 (2007/10/02)

Anodic oxidation of β-oxocarboxylate cyclic acetals in anhydrous methanol gives 2-methoxy-1,4-dioxacycloalkanes in 40-60percent yields. The mechanism is discussed.

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