190191-53-8 Usage
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the compound, which is 10 carbons, 10 hydrogens, and 4 oxygens.
2. Carboxylic Acid Derivative
Explanation
It is a compound derived from a carboxylic acid, which contains a -COOH functional group.
Explanation
A phenyl group (C6H5) is attached to the second carbon atom in the 1,3-dioxane ring structure.
Explanation
The compound contains a six-membered dioxane ring, which consists of two oxygen atoms and four carbon atoms.
5. Trans-Configuration
Explanation
The "trans-" prefix indicates that the phenyl group and the carboxylic acid functional group are on opposite sides of the dioxane ring, resulting in a specific spatial arrangement.
Explanation
Due to its unique structure and properties, the compound may have potential uses in these industries, although further research is needed to confirm its applications and effects.
Explanation
More investigation is required to fully comprehend the compound's potential applications, benefits, and any possible side effects or drawbacks.
Phenyl Group Attachment
2nd carbon atom of the dioxane ring
Dioxane Ring
1,3-Dioxane
Potential Applications
Pharmaceutical or chemical industries
Further Research
Necessary for understanding potential uses and effects
Check Digit Verification of cas no
The CAS Registry Mumber 190191-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,1,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 190191-53:
(8*1)+(7*9)+(6*0)+(5*1)+(4*9)+(3*1)+(2*5)+(1*3)=128
128 % 10 = 8
So 190191-53-8 is a valid CAS Registry Number.
190191-53-8Relevant academic research and scientific papers
Conformational Analysis of 5-Substituted 1,3-Dioxanes. 7. Effect of Lithium Bromide Addition
Juaristi, Eusebio,Díaz, Francisco,Cuéllar, Geiser,Jiménez-Vázquez, Hugo A.
, p. 4029 - 4035 (2007/10/03)
The position of equilibria, established by means of BF3, between diastereomeric cis- and trans-5- substituted-2-phenyl-1,3-dioxanes, in solvents THF and CHCl3, and in the presence of 0, 1, and 10 equiv of LiBr has been determined. The observed ΔG° values show that the addition of salt to the reaction medium influences the position of equilibrium. Lithium bromide effects on the conformational behavior are discussed in terms of lithium ion complexation events that lead to increased stability of the axial isomers when the substituent at C(5) is CO2H, CO2CH3, CONHCH3, and CH2- OH. By contrast, disruption of the intramolecular hydrogen bond present in the axial 5-acetamido derivative (cis-9 substituent equal to NHCOCH3) modifies the preference for the axial conformation in salt-free 9 to a net dominance of the equatorial isomer in the presence of LiBr. Interpretation of the experimental observations was based on models that are apparently supported by semiempirical AM1 calculations. The results derived from the present study contribute to our understanding of the processes involved in molecular recognition and may model salt effects in physiological events.
