109282-37-3 Usage
Uses
Used in Organic Synthesis:
(1R,4S,5R,6S)-1,4-dimethyl-7-oxabicyclo[2.2.1]heptane-5,6-dicarboxylic acid serves as a valuable intermediate in organic synthesis due to its unique structural features and the reactivity of its carboxylic acid groups. It can be used to construct more complex organic molecules through various chemical reactions.
Used in Pharmaceutical Research:
(1R,4S,5R,6S)-1,4-dimethyl-7-oxabicyclo[2.2.1]heptane-5,6-dicarboxylic acid's distinctive stereochemistry and functional groups make it a candidate for pharmaceutical research. It may be utilized in the development of new drugs, particularly those targeting specific biological receptors or enzymes, due to its potential to form stable complexes or engage in specific interactions.
Used in Chiral Chemistry:
Given its four chiral centers, (1R,4S,5R,6S)-1,4-dimethyl-7-oxabicyclo[2.2.1]heptane-5,6-dicarboxylic acid can be employed in chiral chemistry to study the effects of stereochemistry on chemical reactions and biological activities. This can lead to advancements in understanding the role of stereochemistry in drug efficacy and selectivity.
Used in Material Science:
(1R,4S,5R,6S)-1,4-dimethyl-7-oxabicyclo[2.2.1]heptane-5,6-dicarboxylic acid's structural attributes may also find applications in material science, potentially contributing to the development of new materials with specific properties, such as polymers with tailored characteristics for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 109282-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,2,8 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109282-37:
(8*1)+(7*0)+(6*9)+(5*2)+(4*8)+(3*2)+(2*3)+(1*7)=123
123 % 10 = 3
So 109282-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O5/c1-9-3-4-10(2,15-9)6(8(13)14)5(9)7(11)12/h5-6H,3-4H2,1-2H3,(H,11,12)(H,13,14)/t5-,6+,9-,10+
109282-37-3Relevant articles and documents
Stereoselective Syntheses of 3-Acetyl-1,2-dimethyl-1-cyclopentanols. Syntheses of dl-Plinols A, B, and C
Imagawa, Takeshi,Matsuura, Kazuyuki,Murai, Nobuyuki,Akiyama, Tetsuo,Kawanisi, Mituyosi
, p. 3020 - 3022 (2007/10/02)
c- and t-3-Acetyl-1,c-2-dimethyl-r-1-cyclopentanols and c-3-acetyl-1,t-2-dimethyl-r-1-cyclopentanol are synthesized stereoselectively and dl-plinols A, B, and C are prepared therefrom.
