5436-91-9 Usage
Uses
Used in Pesticide and Herbicide Applications:
2-(2,4-dichlorophenyl)-1,3-dioxane is utilized as an active ingredient in pesticides and herbicides, where it serves to inhibit the growth of unwanted plants and organisms. Its effectiveness in controlling plant growth makes it a valuable tool in agricultural and horticultural practices.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, 2-(2,4-dichlorophenyl)-1,3-dioxane is employed as an intermediate in the synthesis of various organic compounds, contributing to the development of new drugs and medicinal products.
Used in Organic Compound Synthesis:
Beyond its applications in pharmaceuticals, 2-(2,4-dichlorophenyl)-1,3-dioxane is also used in the synthesis of other organic compounds, highlighting its versatility in chemical processes.
It is crucial to handle 2-(2,4-dichlorophenyl)-1,3-dioxane with caution due to its potential harmful effects if ingested or inhaled, and its ability to cause skin and eye irritation. Proper safety measures should be taken during its use to mitigate these risks.
Check Digit Verification of cas no
The CAS Registry Mumber 5436-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5436-91:
(6*5)+(5*4)+(4*3)+(3*6)+(2*9)+(1*1)=99
99 % 10 = 9
So 5436-91-9 is a valid CAS Registry Number.
5436-91-9Relevant academic research and scientific papers
Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions
Aliyan, Hamid,Fazaeli, Razieh,Massah, Ahmad Reza,Momeni, Ahmad Reza,Naghash, Hamid Javaherian,Moeinifard, Behzad
experimental part, p. 873 - 876 (2012/04/05)
Carbonyl compounds were converted to the corresponding 1,3-dioxolanes and 1,3-dioxanes with ethylene glycol and 1,3-propandiol in the presence of bismuth triflate under solvent-free conditions. In addition, high chemoselective protection of aldehydes in the presence of ketones has been achieved.
Highly efficient and chemoselective acetalization of carbonyl compounds catalyzed by new and reusab e zirconyl triflate, zr0(0tf)2
Moghadam, Majid,Mohammadpoor-Baltork, Iraj,Tangestaninejad, Shahram,Mirkhani, Valiollah,Yazdani, Parvin,Ghorjipoor, Saeedeh
experimental part, p. 131 - 135 (2009/09/30)
Various types of aromatic aldehydes were efficiently converted to their corresponding 1,3-dioxanes and 1,3-dioxolane with 1,3-propanediol and ethylene glycol, respectively, in the presence of catalytic amount of ZrO(OTf) 2 in acetonitrile at room temperature. The catalyst can be reused several times without loss of its catalytic activity. Very short reaction times, selective acetalization of aromatic aldehydes in the presence of aliphatic aldehydes and ketones, very mild reaction conditions, reusability of the catalyst, and easy workup are noteworthy advantages of this method.
