717888-68-1 Usage
Class
Dioxolanes
It belongs to the class of dioxolane compounds, which are cyclic ethers with two oxygen atoms in the ring.
Stereochemistry
(3R,5R)-rel
The stereochemistry of this compound is specified as (3R,5R)-rel, indicating the arrangement of atoms in the 3rd and 5th positions of the molecule.
Dioxolan ring
A four-membered ring containing two oxygen atoms.
Hydroxyl group (-OH)
A hydroxyl group is present at the 3rd position of the dioxolan ring.
Methoxy group (-OCH3)
A methoxy group is attached to the 5th position of the dioxolan ring.
Dimethyl groups
Two methyl groups are present at the 3rd and 5th positions of the dioxolan ring.
Solubility
Likely soluble in organic solvents such as ethanol, methanol, and dichloromethane.
Boiling point
The exact boiling point is not provided, but it can be estimated based on the molecular size and functional groups.
Melting point
The exact melting point is not provided, but it can be estimated based on the molecular size and functional groups.
Organic synthesis
Due to its unique structure and reactivity, it may be used as an intermediate in the synthesis of other organic compounds.
Pharmaceutical research
Its potential applications in the development of new drugs or drug candidates are yet to be explored.
Further research
More research is needed to fully understand the potential uses, effects, and reactivity of this compound in various chemical and biological contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 717888-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,7,8,8 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 717888-68:
(8*7)+(7*1)+(6*7)+(5*8)+(4*8)+(3*8)+(2*6)+(1*8)=221
221 % 10 = 1
So 717888-68-1 is a valid CAS Registry Number.
717888-68-1Relevant articles and documents
Ozonolysis of 1,4-cyclohexadienes in the presence of methanol and acid. Mechanism and intermediates in the conversion of 1,4-cyclohexadiene derivatives to β-keto esters
Gbara-Haj-Yahia, Isra,Zvilichovsky, Gury,Seri, Noa
, p. 4135 - 4139 (2004)
Conditions for the preparation of β-keto esters directly from 1,4-cyclohexadiene derivatives are described. This procedure is a further step in the application of the synthetic methodology, which consists of the combination of Birch reduction of available benzene derivatives followed by ozonolysis. In this work, the syntheses of derivatives of dimethyl γ-keto-α-aminoadipate and dimethyl β-keto glutamate from the corresponding 1,4-cyclohexadiene derivatives are described. The latter compounds are prepared from phenylalanine and phenylglycine, respectively. The study of the ozonolysis of simple alkyl derivatives of 1,4-cyclohexadiene in the presence of methanol, both in the presence and absence of acid, helped to establish the mechanism of this reaction. The proximity of the two double bonds, which are cleaved, leads to the intermediate formation of 1,2-dioxolane derivatives that could be identified by NMR spectroscopy. It is shown that regardless of the regioselectivity of the cleavage of the primary ozonide, which is formed, all 1,2-dioxolane derivatives can lead to β-keto esters. This is due to the equilibrium between these dioxolanes in the presence of methanol and acid.
