22924-16-9 Usage
General Description
2,4-diethoxy-benzaldehyde is a chemical compound with the formula C10H14O3. It is a pale yellow liquid with a strong, sweet, floral odor. 2,4-diethoxy-benzaldehyde is a derivative of benzaldehyde and is commonly used as a building block in the synthesis of pharmaceuticals and fine chemicals. It is also used as a flavoring agent in the food industry. Additionally, it has been found to have potential pharmacological activities, such as anti-inflammatory and analgesic properties. However, it should be handled with caution, as it is flammable and may be harmful if swallowed, inhaled, or in contact with skin.
Check Digit Verification of cas no
The CAS Registry Mumber 22924-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,2 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22924-16:
(7*2)+(6*2)+(5*9)+(4*2)+(3*4)+(2*1)+(1*6)=99
99 % 10 = 9
So 22924-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O3/c1-3-13-10-6-5-9(8-12)11(7-10)14-4-2/h5-8H,3-4H2,1-2H3
22924-16-9Relevant articles and documents
Use of o-hydroxy-p-methoxybenzaldehyde derivative as herbicide
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Paragraph 0008; 0011; 0014; 0043; 0047-0048, (2021/04/10)
The invention discloses an application of an o-hydroxy p-methoxybenzaldehyde derivative as a herbicide. The o-hydroxy-p-methoxybenzaldehyde derivative and the herbicide taking the o-hydroxy-p-methoxybenzaldehyde derivative as a component are used for preventing and removing weeds in a field crop growth place and a non-farming crop place.
Stepwise degradation of hydroxyl compounds to aldehydes: Via successive C-C bond cleavage
Liu, Mingyang,Zhang, Zhanrong,Shen, Xiaojun,Liu, Huizhen,Zhang, Pei,Chen, Bingfeng,Han, Buxing
supporting information, p. 925 - 928 (2019/01/24)
Stepwise degradation of hydroxyl compounds to aldehydes via successive cleavage of C-C bonds was achieved by using a bimetallic catalytic system (PdCl2 + CuCl) without any ligands and additives. The broad applicability is expanded to a diverse range of aromatic, aliphatic, primary and secondary alcohols, as well as lignin model compounds.
