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Benzoic acid, 4-(methoxymethoxy)-, ethyl ester, also known as ethyl 4-(methoxymethoxy)benzoate, is an organic compound with the chemical formula C11H14O4. It is a colorless liquid with a molecular weight of 210.23 g/mol. This ester derivative of benzoic acid is characterized by the presence of a methoxymethoxy group (-OCH2OCH3) at the para position of the benzene ring and an ethoxy group (-OCH2CH3) at the carboxylic acid end. It is synthesized by reacting 4-hydroxybenzoic acid with ethyl orthoformate, and it is used as a chemical intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is sensitive to light and heat, and it is typically stored in a cool, dry place away from direct sunlight.

5942-30-3

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5942-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5942-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5942-30:
(6*5)+(5*9)+(4*4)+(3*2)+(2*3)+(1*0)=103
103 % 10 = 3
So 5942-30-3 is a valid CAS Registry Number.

5942-30-3Relevant academic research and scientific papers

First total synthesis of mariamide A

Xia, Yamu,Chen, Chenglong,Li, Mengying,Zhou, Weizeng,Sun, Shuyu,Chu, Shanpeng,Wang, Hui

, p. 114 - 120 (2019/12/12)

Mariamide A, a lignanamide isolated from the seeds of Silybum marianum, has demonstrated potential utility as an antioxidant and antidiabetic agent and possesses an 8-O-4′ neolignan skeleton. Herein, a first total synthesis of mariamide A is presented that proceeds in nine steps using vanillin as the starting material. The key steps for the preparation of mariamide A involve an I2-catalyzed bromomethoxylation of an alkene group, a nucleophilic substitution followed by a sequential elimination and a monoacylation reaction.

Polymerizable liquid crystal compound, and optical antisotropic compsn.

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Paragraph 0070, (2016/10/10)

The present description relates to a polymerizable liquid crystal compound, a polymerizable liquid crystal composition including the same, and an optically anisotropic body. The polymerizable liquid crystal compound includes a radical derived from the first liquid crystal molecule including a mesogen group having a non-aromatic ring; a radical derived from the second liquid crystal molecule including a mesogen group that has a structure different from said mesogen group having a non-aromatic ring and includes a ring containing a double bond; and a linker that has a specific structure and links the sp3-hybridized carbon in the non-aromatic ring of the radical derived from the first liquid crystal molecule and the sp2-hybridized carbon in the mesogen group of the radical derived from the second liquid crystal molecule, wherein at least one of the radicals derived from the first and the second liquid crystal molecules may include one or more polymerizable groups which are connected to the mesogen group directly or via spacer groups. Such polymerizable liquid crystal compound makes it possible to exhibit stable reverse wavelength dispersion solely or by being mixed with other liquid crystal materials.

A One-Step Conversion of p-Methoxybenzyl Ethers into Methoxymethyl Ethers by the Action of Dimethoxymethane in the Presence of Tin(II) Bromide and Bromomethyl Methyl Ether

Oriyama, Takeshi,Kimura, Mikio,Koga, Gen

, p. 885 - 887 (2007/10/02)

The combined use of dimethoxymethane with catalytic amounts of tin(II) bromide and bromomethyl methyl ether cleaves p-methoxybenzyl ethers to give methoxymethyl ethers in good yields.The chemoselective conversion of p-methoxybenzyl ethers in the presence of the benzyl ether function into methoxymethyl ethers has also occurred successfully.

Prediction of the Absolute Configuration of Optically Active Pheromones Using Liquid Crystals

Ikemoto, Tetsuya,Mitsuhashi, Kazuhiro,Mori, Kenji

, p. 687 - 694 (2007/10/02)

Prediction of the absolute configuration of optically active methyl branched pheromones is possible by combining them with mesogens to give them liquid crystalline properties and measuring the helical senses of the chiral nematic phases.

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