36056-90-3 Usage
Description
Ethyl 3,3-diethoxy-2-Methylpropanoate is an organic compound characterized by the chemical formula C9H18O4. It is a colorless liquid with a distinctive fruity aroma, known for its low toxicity and pleasant scent. Ethyl 3,3-diethoxy-2-Methylpropanoate is recognized for its safety in various applications, earning it the status of Generally Recognized As Safe (GRAS) by the Food and Drug Administration (FDA) in the United States.
Uses
Used in the Food and Beverage Industry:
Ethyl 3,3-diethoxy-2-Methylpropanoate is employed as a flavoring agent, enhancing the taste and aroma of various food and beverage products. Its fruity scent and safety profile make it a preferred choice for adding flavor without compromising the quality or safety of the final product.
Used in Fragrance and Perfume Industry:
Ethyl 3,3-diethoxy-2-Methylpropanoate is also utilized in the production of fragrances and perfumes, where its fruity odor contributes to creating appealing scents for personal care and cosmetic products. Its use in these applications is supported by its low toxicity and pleasant olfactory characteristics.
Used in Industrial Processes as a Solvent:
Ethyl 3,3-diethoxy-2-Methylpropanoate serves as a solvent in various industrial applications, facilitating processes that require the dissolution of other substances. Its properties make it suitable for use in a range of manufacturing and chemical processes, contributing to the production of diverse consumer goods.
Check Digit Verification of cas no
The CAS Registry Mumber 36056-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,5 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36056-90:
(7*3)+(6*6)+(5*0)+(4*5)+(3*6)+(2*9)+(1*0)=113
113 % 10 = 3
So 36056-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O4/c1-5-12-9(11)8(4)10(13-6-2)14-7-3/h8,10H,5-7H2,1-4H3
36056-90-3Relevant articles and documents
Syntheses of 4-[(1H,3H)-pyrimidine-2,4-dion-1-yl]- and 4-[(1H,3H)-5- methylpyrimidine-2,4-dion-1-yl]-1,6-heptadienes
Bouhadir, Kamal H.,Zhou, Jing-Lan,Shevlin, Philip B.
, p. 1003 - 1010 (2007/10/03)
Heptadienes containing nucleic bases are attractive building blocks for the synthesis of carbocyclic oligonucleotide analogs. Herein, we report an alternative synthetic route to 4-[(1H,3H)-pyrimidine-2,4-dion-1-yl]-1,6- heptadiene and 4-[(1H,3H)-5-methylpyrimidine-2,4-dion-1-yl]-1,6-heptadiene via building the pyrimidine ring utilizing 4-isocyanato-1,6-heptadiene intermediate.
2-Benzazepines. 8. Zerovalent nickel mediated biaryl synthesis of an anxiolytic pyrimido[5,4-d][2]benzazepine
Coffen,Schaer,Bizzarro,Cheung
, p. 296 - 300 (2007/10/02)
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