139892-53-8 Usage
Description
(R)-2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane is an organochlorine compound with a unique spiro structure, featuring a ten-membered carbon ring fused to a four-membered dioxane ring. The chlorine atom is positioned at the second position of the spiro junction, and the (R) stereoisomer indicates the specific spatial configuration of the molecule.
Uses
Used in Chemical Synthesis:
(R)-2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane is used as a building block or intermediate in the synthesis of various complex organic molecules. Its unique spiro structure and functional groups make it a valuable component in the development of new chemical compounds.
Used in Pharmaceutical Industry:
(R)-2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane is used as a key intermediate in the synthesis of pharmaceutical compounds. Its structural features may contribute to the development of new drugs with potential therapeutic applications.
Used in Material Science:
(R)-2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane is used as a component in the development of novel materials with specific properties, such as improved stability, reactivity, or selectivity. Its unique molecular structure may play a crucial role in the design and synthesis of advanced materials for various applications.
Note: The specific applications and industries mentioned above are hypothetical and provided as examples. Further research and information from specialized databases or chemical catalogues are necessary to determine the actual uses and roles of (R)-2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 139892-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,8,9 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139892-53:
(8*1)+(7*3)+(6*9)+(5*8)+(4*9)+(3*2)+(2*5)+(1*3)=178
178 % 10 = 8
So 139892-53-8 is a valid CAS Registry Number.
139892-53-8Relevant articles and documents
Enzymatic resolution of 2,2-disubstituted-1,3-dioxolane-4-methanol carboxylic esters
Partali,Melbye,Alvik,Anthonsen
, p. 65 - 72 (2007/10/02)
The enantioselectivity of enzymatic hydrolysis of carboxylic esters of various 1,2-ketals of glycerol has been investigated. The influence of the ketal group has been studied. A number of lipases and proteinases have been tested and the best enantioselectivity was obtained with proteinase from Aspergillus oryzae which gave an E-value of 9 with 2,2-dimethyl-1,3-dioxolane-4-methanol butanoate. Variations in the acyl part revealed that butanoyl was optimal. All hydrolysis products have been synthesised in homochiral forms from homochiral starting materials.
