69469-91-6 Usage
Description
1-(2-hydroxy-4-methoxy-3-methylphenyl)ethanone, also known as Vanillin acetophenone, is a chemical compound with a molecular formula C10H12O3. It is characterized by its sweet, vanilla-like aroma and is commonly synthesized from vanillin and acetyl chloride.
Uses
Used in the Food Industry:
1-(2-hydroxy-4-methoxy-3-methylphenyl)ethanone is used as a flavoring agent for its sweet, vanilla-like aroma, enhancing the taste and aroma of various food products such as chocolate, confectionery, and baked goods.
Used in the Pharmaceutical Industry:
1-(2-hydroxy-4-methoxy-3-methylphenyl)ethanone has potential applications in the pharmaceutical industry, with ongoing research being conducted to explore its diverse properties and potential uses. Its specific role and application in this industry are still under investigation.
Used in the Cosmetic Industry:
Similarly, 1-(2-hydroxy-4-methoxy-3-methylphenyl)ethanone is being explored for its potential applications in the cosmetic industry. The research aims to determine its suitability and effectiveness in various cosmetic products, taking advantage of its unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 69469-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,6 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69469-91:
(7*6)+(6*9)+(5*4)+(4*6)+(3*9)+(2*9)+(1*1)=186
186 % 10 = 6
So 69469-91-6 is a valid CAS Registry Number.
69469-91-6Relevant articles and documents
Studies in synthesis and tautomerism of new warfarin derivatives
Soman, Shubhangi S.,Patel,Jethawa, Komal B.,Baloni, Radhika
, p. 233 - 236 (2013/09/24)
Substituted 4-hydroxy-7-methoxy-benzopyran-2-(/-V)-one on Michael condensation with different a,p-unsaturated ketones gave various warfarin derivatives. 1H NMR studies of these compounds in deuteriochloroform showed three interconverting tautomeric structures, two of which are cyclic diastereomeric hemiketals, while the third one is the open chain intermediate form; whereas the 1H NMR in deuteriodimethylsulfoxide shows existence of only two diastereomeric hemiketal forms.
Synthesis of a Diels-Alder precursor for the Elisabethin A skeleton
Heckrodt, Thilo J.,Mulzer, Johann
, p. 1857 - 1866 (2007/10/03)
A synthesis of a precursor 2 for the Elisabethin A skeleton is reported. Containing a masked quinone and a (E,Z)-diene sub-unit, it has the required elements for the envisaged intramolecular Diels-Alder reaction to form the tricyclic system of Elisabethin A. Starting from methylresorcinol, the sequence involves the preparation of an arylacetic acid, which was α-alkylated by a chiral building block. Subsequent HWE reaction and cis-selective Wittig olefination furnished the diene with the desired geometry.
