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2-Ethyl hexanal and cycloglycol acetal are two distinct chemicals with different properties and applications. 2-Ethyl hexanal is an organic compound with a molecular formula of C8H16O, characterized by its aldehyde functional group and a six-carbon chain with an ethyl group attached to the second carbon. It is a colorless liquid with a strong, fruity odor and is commonly used as a flavoring agent in the food and beverage industry, particularly in the production of artificial fruit flavors. On the other hand, cycloglycol acetal, also known as 1,4-dioxane, is a cyclic ether with the molecular formula C4H8O2. It is a colorless, volatile liquid that is miscible with water and various organic solvents. Cycloglycol acetal is primarily used as a solvent in the chemical industry, particularly in the production of polymers and resins. It is also employed as a stabilizer for chlorinated solvents and as a component in some paint removers. Both chemicals have their unique applications and properties, making them valuable in their respective industries.

4359-47-1

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4359-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4359-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4359-47:
(6*4)+(5*3)+(4*5)+(3*9)+(2*4)+(1*7)=101
101 % 10 = 1
So 4359-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O2/c1-3-5-6-9(4-2)10-11-7-8-12-10/h9-10H,3-8H2,1-2H3

4359-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-heptan-3-yl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane,2-(1-ethylpentyl)

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:4359-47-1 SDS

4359-47-1Relevant academic research and scientific papers

Visible-light-induced acetalization of aldehydes with alcohols

Yi, Hong,Niu, Linbin,Wang, Shengchun,Liu, Tianyi,Singh, Atul K.,Lei, Aiwen

supporting information, p. 122 - 125 (2017/11/27)

In this work, we have achieved a simple and general method for acetalization of aldehydes by means of a photochemical reaction under low-energy visible light irradiation. A broad range of aromatic, heteroaromatic, and aliphatic aldehydes have been protected under neutral conditions in good to excellent yields using a catalytic amount of Eosin Y as the photocatalyst. Our visible light mediated acetalization strategies are successful for more challenging acid-sensitive aldehydes and sterically hindered aldehydes. Notably, this protocol is chemoselective to aldehydes, while ketones remain intact.

Cyclopentyl methyl ether-NH4X: A novel solvent/catalyst system for low impact acetalization reactions

Azzena, Ugo,Carraro, Massimo,Mamuye, Ashenafi Damtew,Murgia, Irene,Pisano, Luisa,Zedde, Giuseppe

supporting information, p. 3281 - 3284 (2015/06/25)

Cyclopentyl methyl ether, a low impact ether forming a positive azeotrope with water, was successfully employed as a solvent in the synthesis of 1,3-dioxanes and 1,3-dioxolanes carried out under Dean-Stark conditions by the acetalization of aliphatic and aromatic aldehydes or ketones, employing ammonium salts as environmentally friendly acidic catalysts.

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