32917-26-3 Usage
Molecular Weight
258.28 g/mol
Functional Groups
Ester, Carboxylic Acid, and Spiro
Ketal
A ketal is a type of acetal that is formed by the reaction of a ketone with an alcohol.
Ester
An ester is a compound derived from an acid (in this case, the carboxylic acid) in which at least one hydroxyl group is replaced by an alkoxy group.
Medicinal and Pharmaceutical Research
Due to its unique structural properties, it may be used in the synthesis of various pharmaceutical compounds.
Drug Development
It may have potential applications in drug development.
Industrial Uses
It may also have industrial uses due to its properties and reactivity.
Further Research
Further research and testing are needed to fully understand its potential applications and effects.
Solubility
The solubility of this compound is not mentioned in the provided material, but it is likely to be soluble in organic solvents like ethanol, methanol, or acetone.
Stability
The stability of this compound is not mentioned in the provided material, but it is likely to be stable under normal conditions, as it is a common compound used in research.
Reactivity
The reactivity of this compound is not mentioned in the provided material, but it is likely to be reactive due to the presence of functional groups like ester and carboxylic acid.
Check Digit Verification of cas no
The CAS Registry Mumber 32917-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,1 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32917-26:
(7*3)+(6*2)+(5*9)+(4*1)+(3*7)+(2*2)+(1*6)=113
113 % 10 = 3
So 32917-26-3 is a valid CAS Registry Number.
32917-26-3Relevant articles and documents
A Stereoselective Synthesis of (+/-)-Homogynolide-B
Srikrishna, Adusumilli,Nagaraju, Sankuratri,Venkateswarlu, Somepalli
, p. 429 - 432 (1994)
A highly stereoselective formal total sysnthesis of homogynolide-B via the ketoketals 4 and the ketospirolactone 3a starting from Hagemann's ester 2 is describe .
Regioselective synthesis of bicyclo[4.2.1]nonane-2,8-diones via BF3.ET2O mediated intramolecular diazo ketone insertion reaction
Srikrishna,Ramachary
, p. 1605 - 1606 (2007/10/03)
Treatment of the diazo diones 11a-d with boron trifluoride diethyl etherate furnished the bicyclo[4.2.1]nonane-2,8-diones 15a-d in a highly regioselective manner.
SYNTHESIS OF SOME DERIVATIVES OF CYCLOHEXANECARBOXYLIC ACID AND THEIR MESOMORPHOUS CHARACTERISTICS.
Bezborodov, V. S.
, p. 1148 - 1152 (2007/10/02)
The cis- and trans-4-(4-methoxyphenyl)cyclohexane-1-carboxylic, cis-4-(4-methoxyphenyl)-cis-2-methylcyclohexane-1-r-carboxylic, and trans-4-(4-methoxyphenyl)-trans-2-methylcyclohexane-1-r-carboxylic acids and their 4-cyanophenyl esters were obtained.Unlik
