4362-48-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of 1,3-Dioxolane, 2-cyclohexyl-.
Explanation
The chemical structure describes the arrangement of atoms and the type of bonds between them in the compound.
Explanation
1,3-Dioxolane, 2-cyclohexylis used as a solvent due to its ability to dissolve a wide range of substances, making it useful in various industries.
Explanation
As a reactant, 1,3-Dioxolane, 2-cyclohexylparticipates in chemical reactions to form new compounds, which can be used in the production of various products.
Explanation
Acute toxicity refers to the harmful effects of a substance when it is absorbed by the body in a short period. Low acute toxicity means that the compound is less likely to cause severe harm during short-term exposure.
Explanation
Although the compound has low acute toxicity, long-term exposure or ingestion can still lead to health issues, such as irritation in the mentioned body parts.
Explanation
To minimize the risk of health issues, it is essential to follow safety guidelines and protocols when working with this chemical compound.
Chemical structure
Cyclic ether with a dioxolane ring and a cyclohexyl group
Industrial applications
Solvent in manufacturing of pharmaceuticals, pesticides, and other organic compounds
Use in organic synthesis
Reactant in organic synthesis
Component in synthetic flavorings
Used in the creation of artificial flavors
Low acute toxicity
Known to have low acute toxicity
Potential health risks
Prolonged exposure or ingestion may cause irritation to the respiratory system, skin, and eyes
Safety precautions
Proper safety measures should be taken when handling 1,3-Dioxolane, 2-cyclohexyl-
Check Digit Verification of cas no
The CAS Registry Mumber 4362-48-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4362-48:
(6*4)+(5*3)+(4*6)+(3*2)+(2*4)+(1*8)=85
85 % 10 = 5
So 4362-48-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h8-9H,1-7H2
4362-48-5Relevant articles and documents
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.
Acid-free, organocatalytic acetalization
Kotke, Mike,Schreiner, Peter R.
, p. 434 - 439 (2007/10/03)
The acid-free, organocatalytic acetalization of various aldehydes and ketones with N,N′-bis[3,5-bis(trifluoromethyl)phenyl]thiourea is presented. The neutral, double hydrogen bonding thiourea catalyst can be used at very low loadings of 0.01-1 mol% at room temperature to furnish the respective acetals in 65-99% yield at turnover frequencies around 600 h-1. Acid-labile TBDMS-protected as well as unsaturated aldehydes can be converted efficiently into their acetals utilizing this very mild and highly practical method.
Highly shape-selective, biomimetic, and efficient deprotection of carbonyl compounds masked as ethylene acetals or dioxolanes produced from 1,2-ethanediol
Ji, Hong-Bing
, p. 3659 - 3662 (2007/10/03)
A simple, mild, efficient, and organic solvent-free biochemical approach for the deprotection of carbonyl compounds protected as 1,3-dioxolanes through the use of cyclodextrins as catalysts has been developed. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.