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53951-43-2

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53951-43-2 Usage

Description

2,4-Dimethyl-1,3-dioxolane-2-methanol, also known as 2,4-Dimethyl-2-methylol-1,3-dioxolane, is an organic compound with the molecular formula C6H12O3. It features a dioxolane ring with two methyl groups at the 2nd and 4th positions and a hydroxymethyl group at the 2nd position. 2,4-Dimethyl-1,3-dioxolane-2-methanol is known for its stability and reactivity in various chemical reactions, making it a valuable component in organic synthesis.

Uses

Used in Organic Synthesis:
2,4-Dimethyl-1,3-dioxolane-2-methanol is used as a research reagent for organic synthesis due to its unique structural features and reactivity. It serves as a versatile building block in the creation of complex organic molecules and compounds, contributing to the advancement of chemical research and development.
Used in Chemical Processes:
In addition to its role in organic synthesis, 2,4-Dimethyl-1,3-dioxolane-2-methanol is also utilized in various chemical processes. Its stability and reactivity make it a suitable candidate for use in the production of different chemicals, pharmaceuticals, and materials, further expanding its applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 53951-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,5 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53951-43:
(7*5)+(6*3)+(5*9)+(4*5)+(3*1)+(2*4)+(1*3)=132
132 % 10 = 2
So 53951-43-2 is a valid CAS Registry Number.

53951-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-dimethyl-1,3-dioxolan-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane-2-methanol,2,4-dimethyl

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:53951-43-2 SDS

53951-43-2Upstream product

53951-43-2Downstream Products

53951-43-2Relevant articles and documents

Selectivity Switch in the Aerobic 1,2-Propandiol Oxidation Catalyzed by Diamine-Stabilized Palladium Nanoparticles

Oberhauser, Werner,Evangelisti, Claudio,Capozzoli, Laura,Manca, Gabriele,Casaletto, Maria Pia,Vizza, Francesco

, p. 2896 - 2906 (2021/05/06)

Palladium nanoparticles stabilized by a sterically demanding secondary diamine ligand have been synthesized by hydrogen reduction of a palladium acetate complex bearing the corresponding diimine ligand. The obtained nanoparticles were used to catalyze the aerobic oxidation of 1,2-propandiol in n-hexane, and after their heterogenization onto a high surface area carbon, in water. In n-hexane (2,4-dimethyl-1,3-dioxolan-2-yl) methanol has been obtained as major product, whereas in water acetic acid with a selectivity of >85 % has been achieved. The selectivity switch observed was a clear induced by water. The robustness of diamine-stabilized palladium nanoparticles under real aerobic oxidation conditions has been proved by recycling experiments, TEM measurements of the recovered catalysts and by comparison of its performance with that of palladium nanoparticles generated by the metal vapor synthesis technique and supported onto the same carbon in the absence of the stabilizing diamine ligand.

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