40630-71-5 Usage
Uses
Used in Organic Synthesis:
2-(((2,2-diMethyl-1,3-dioxolan-4-yl)Methoxy)carbonyl)benzoic acid is used as a key intermediate in organic synthesis for its ability to react with other compounds, facilitating the creation of new chemical entities.
Used in Pharmaceutical Research and Drug Design:
In the pharmaceutical industry, 2-(((2,2-diMethyl-1,3-dioxolan-4-yl)Methoxy)carbonyl)benzoic acid is utilized as a building block in drug design and development. Its unique structure allows for the formation of complex organic molecules with potential therapeutic properties.
Used in the Synthesis of Complex Organic Molecules:
2-(((2,2-diMethyl-1,3-dioxolan-4-yl)Methoxy)carbonyl)benzoic acid is employed as a versatile component in the synthesis of complex organic molecules, contributing to the advancement of chemical research and the discovery of novel compounds with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40630-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,3 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40630-71:
(7*4)+(6*0)+(5*6)+(4*3)+(3*0)+(2*7)+(1*1)=85
85 % 10 = 5
So 40630-71-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O6/c1-14(2)19-8-9(20-14)7-18-13(17)11-6-4-3-5-10(11)12(15)16/h3-6,9H,7-8H2,1-2H3,(H,15,16)
40630-71-5Relevant academic research and scientific papers
Synthesis of (R)- and (S)-isopropylidene glycerol
Pallavicini,Valoti,Villa,Piccolo
, p. 5 - 8 (2007/10/02)
The preparation of (R)- and (S)-isopropylidene glycerol 1 of high enantiomeric excess (> 98%) was accomplished through salt formation between their hydrogen phthalates with (S)- and (R)-1-methylbenzylamine [MBA] respectively, selective crystallization of these salts and subsequent regeneration of optically active compounds 1 by saponification. The progress of resolution was followed by HPLC analysis on Chiralcel OJ, after converting the hydrogen phthalates into the corresponding mono methyl esters by diazomethane.
