191354-59-3 Usage
Explanation
The full name of the compound, indicating its structure and stereochemistry.
Explanation
The compound is a specific stereoisomer, with the (S) configuration, which refers to the spatial arrangement of atoms in the molecule.
Explanation
The compound contains an ester functional group, a phenyl group (a six-carbon ring attached to a benzene ring), and a 1,3-dioxolane group (a five-membered heterocyclic ring with oxygen atoms).
Explanation
The molecular structure of the compound includes a carbonyl group (C=O), an ester linkage (C-O-C), and aromatic rings from the phenyl and benzene groups.
Explanation
The compound is derived from 1,3-dioxolane, which is a five-membered heterocyclic ring with two oxygen atoms.
Explanation
It is an organic compound, meaning it primarily consists of carbon and hydrogen atoms.
Explanation
Due to its unique structure and properties, the compound may have various industrial or pharmaceutical applications, such as in the synthesis of drugs or as an intermediate in chemical reactions.
Explanation
As an ester with aromatic and heterocyclic groups, the compound is likely to be soluble in organic solvents like ethanol, methanol, or dichloromethane.
Explanation
The compound is expected to be relatively stable under normal conditions, such as room temperature and atmospheric pressure, due to the presence of stable functional groups and aromatic rings.
Explanation
The ester functional group in the compound may undergo reactions with nucleophiles, acids, or bases, leading to the formation of new compounds or the hydrolysis of the ester linkage.
Stereoisomer
(S)-enantiomer
Functional Groups
Ester, Phenyl, 1,3-Dioxolane
Molecular Structure
Contains a carbonyl group, ester linkage, and aromatic rings
Derived from
1,3-Dioxolane
Type
Organic compound
Industrial/Pharmaceutical Applications
Potential uses
Solubility
Likely soluble in organic solvents
Stability
Relatively stable under normal conditions
Reactivity
May react with nucleophiles, acids, or bases
Check Digit Verification of cas no
The CAS Registry Mumber 191354-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,3,5 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 191354-59:
(8*1)+(7*9)+(6*1)+(5*3)+(4*5)+(3*4)+(2*5)+(1*9)=143
143 % 10 = 3
So 191354-59-3 is a valid CAS Registry Number.
191354-59-3Relevant articles and documents
5-Hydroxy[1,2]oxazinan-3-ones as potential carbapenem and D-ala-D-ala surrogates
Wolfe, Saul,Akuche, Christiana,Ro, Stephen,Wilson, Marie-Claire,Kim, Chan-Kyung,Shi, Zheng
, p. 915 - 936 (2007/10/03)
The title compounds are amino acids whose nitrogen atom is enclosed in a six-membered cyclic hydroxamate bearing a C5-hydroxyl group. They belong to a proposed new family of antibacterial agents targeted to the penicillin receptor. The glycine and alanine members of the family have been synthesized, as racemates, in seven steps from the four-carbon synthon diketene and the tert-butyl esters of N-hydroxyglycine and N-hydroxyalanine. Numerous alternatives to diketene have also been examined, but these lead mainly to five-membered cyclic hydroxamates. The theoretical considerations that have led to this synthetic programme are discussed in some detail. They include analysis of the structures of natural and unnatural penicillin surrogates, analysis of the penicillin pharmacophore, and a treatment of the chemical reaction with which penicillin blocks bacterial cell wall synthesis. The glycine derivative exhibits marginal but real activity vs. Micrococcus luteus. The alanine derivative, which more closely resembles D-ala-D-ala, is fifty times more active. Two five-membered structural isomers of the glycine derivative are inactive.
