39050-39-0 Usage
Uses
Used in Flavor and Fragrance Industry:
2-Methyl-1,3-dioxolane-2-carbaldehyde is used as a flavor and fragrance ingredient for its fruity scent, adding depth and complexity to the aroma profiles of food and beverage products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-Methyl-1,3-dioxolane-2-carbaldehyde serves as an intermediate in the synthesis of various organic compounds and pharmaceuticals, leveraging its reactivity to form complex molecules for medicinal applications.
Used in Organic Chemistry:
As a building block in organic chemistry, 2-Methyl-1,3-dioxolane-2-carbaldehyde is used for its ability to undergo a range of chemical reactions, facilitating the creation of diverse chemical structures and compounds for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 39050-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,5 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39050-39:
(7*3)+(6*9)+(5*0)+(4*5)+(3*0)+(2*3)+(1*9)=110
110 % 10 = 0
So 39050-39-0 is a valid CAS Registry Number.
39050-39-0Relevant academic research and scientific papers
Obringer, Michel,Barbarotto, Marie,Choppin, Sabine,Colobert, Francoise
, p. 3542 - 3545 (2009)
Image Persented Efficient synthesis of the fragment C9-C16 bearing the anti, syn stereotriad of ansamycin antibiotics is described. Key steps for controlling the configuration of the three stereogenic centers involve a stereoselective Reformatsky-type reaction followed by a diastereoselective reduction of a β-ketosulfoxide.
Switchover of diastereofacial selectivity in the condensation reaction of optically active N-sulfinimine with ester enolate
Fujisawa, Tamotsu,Kooriyama, Yuuji,Shimizu, Makoto
, p. 3881 - 3884 (2007/10/03)
Both diastereomers of β-aminoester can be obtained diastereoselectively in the reaction of optically active N-sulfinimine possessing 2-methyl-1,3- dioxolanyl group with ester enolate simply by changing the enolate metal species, additives, and solvents. The β-aminoester can be converted into the corresponding 3-unsubstituted β-lactam.
