157096-53-2 Usage
General Description
2-PROPENAL, 3-(4-(ACETYLOXY)PHENYL)-,(2E) is a chemical compound with the molecular formula C12H12O3. It is also known by the trade name Eugenol acetate and is commonly used as a flavoring agent in the food and beverage industry. 2-PROPENAL, 3-(4-(ACETYLOXY)PHENYL)-,(2E) has a sweet, spicy aroma and is often used in toothpaste, perfumes, and other personal care products. It is also utilized in the manufacturing of pharmaceuticals and as a fragrance additive in various cosmetic products. This chemical compound is derived from the essential oil of cloves and has been shown to have antioxidant and antimicrobial properties. However, it should be handled with care as it can cause skin and eye irritation and may be harmful if ingested or inhaled in large quantities.
Check Digit Verification of cas no
The CAS Registry Mumber 157096-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,0,9 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 157096-53:
(8*1)+(7*5)+(6*7)+(5*0)+(4*9)+(3*6)+(2*5)+(1*3)=152
152 % 10 = 2
So 157096-53-2 is a valid CAS Registry Number.
157096-53-2Relevant articles and documents
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Pearl,Darling
, p. 1266 (1957)
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Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro-analogues by three different strategies
Baranovsky, Alexander,Schmitt, Bettina,Fowler, Daniel J.,Schneider, Bernd
, p. 1019 - 1045 (2007/10/03)
Wittig, aldol and Wittig-Horner reactions have been used to synthesize new diarylheptanoids, which are putative intermediates in phenylphenalenone biosynthesis in plants. The Wittig-Horner approach was most suitable and gave significantly higher yields in comparison with other methods.
A mild synthesis of coumaryl, coniferyl, sinapyl aldehydes and alcohols
Daubresse,Francesch,Mhamdi,Rolando
, p. 369 - 371 (2007/10/02)
Acetylconiferyl aldehyde is obtained from acetylvanillin by a Wittig reaction under phase-transfer conditions; basic hydrolysis gives coniferyl aldehyde, or after reduction with sodium borohydride affords coniferyl alcohol. This method is extended to the sinapyl and coumaryl series.
