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3-(4-Hydroxy-3-methoxy-phenyl)-propionic acid propyl ester, also known as propyl vanillate, is an organic compound derived from vanillic acid. It is a colorless to pale yellow liquid with a molecular formula of C12H16O4 and a molecular weight of 224.25 g/mol. This ester is formed by the esterification of vanillic acid with propanol, resulting in a compound that possesses a pleasant, sweet, and slightly spicy odor. Propyl vanillate is widely used in the flavor and fragrance industry, particularly in the production of food, beverages, and cosmetics, due to its ability to impart a creamy, vanilla-like scent. It is also known for its potential antioxidant properties and is sometimes used as a preservative in certain applications.

4624-23-1

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4624-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4624-23-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,2 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4624-23:
(6*4)+(5*6)+(4*2)+(3*4)+(2*2)+(1*3)=81
81 % 10 = 1
So 4624-23-1 is a valid CAS Registry Number.

4624-23-1Downstream Products

4624-23-1Relevant academic research and scientific papers

Catalytic activation of unstrained C(aryl)–C(aryl) bonds in 2,2′-biphenols

Zhu, Jun,Wang, Jianchun,Dong, Guangbin

, p. 45 - 51 (2018/11/23)

Transition metal catalysis has emerged as an important means for C–C activation that allows mild and selective transformations. However, the current scope of C–C bonds that can be activated is primarily restricted to either highly strained systems or more polarized C–C bonds. In contrast, the catalytic activation of non-polar and unstrained C–C moieties remains an unmet challenge. Here we report a general approach for the catalytic activation of the unstrained C(aryl)–C(aryl) bonds in 2,2′-biphenols. The key is to utilize the phenol moiety as a handle to install phosphinites as a recyclable directing group. Using hydrogen gas as the reductant, monophenols are obtained with a low catalyst loading and high functional group tolerance. This approach is also applied to the synthesis of 2,3,4-trisubstituted phenols. A further mechanistic study suggests that the C–C activation step is mediated by a rhodium(i) monohydride species. Finally, a preliminary study on breaking the inert biphenolic moieties in lignin models is illustrated.

Fungicidal activities of dihydroferulic acid alkyl ester analogues

Beck, John J.,Kim, Jong H.,Campbell, Bruce C.,Chou, Shen-Chieh

, p. 779 - 782 (2008/02/12)

The natural product dihydroferulic acid (DFA, 1) and the synthesized DFA methyl (4a), ethyl (4b), propyl (4c), hexyl (4d), octyl (4e), and decyl (4f) esters were examined for antifungal activity. Test fungi included Saccharomyces cerevisiae (wild type, and deletion mutants slt2Δ and bck1Δ), Aspergillus fumigatus, and A. flavus. Growth inhibition of S. cerevisiae treated with 5 mM DFA or the corresponding esters was 4a, 4b, and 4c >98%; 4d 18.8%; 1 6.4%; 4e 6.2%; and 4f 2.8%, relative to the control. The 50% minimum inhibitory concentrations for the more active propyl, methyl, and ethyl esters were 1.5, 2.1, and 4.0 mM, respectively. Compound 4c inhibited 100% growth of both aspergilli at 6.4 mM.

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