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1-(2,4,6-trimethoxyphenyl)propan-2-ol, also known as 2-hydroxy-1-(2,4,6-trimethoxyphenyl)propane, is an organic compound with the molecular formula C12H18O4. It is a colorless to pale yellow liquid with a molecular weight of 226.27 g/mol. 1-(2,4,6-trimethoxyphenyl)propan-2-ol is characterized by a propane-2-ol backbone, with a 2,4,6-trimethoxyphenyl group attached to the first carbon. The presence of three methoxy groups on the phenyl ring gives 1-(2,4,6-trimethoxyphenyl)propan-2-ol unique chemical properties, such as increased solubility in polar solvents and potential applications in the synthesis of various pharmaceuticals and agrochemicals. Due to its complex structure, 1-(2,4,6-trimethoxyphenyl)propan-2-ol is typically synthesized through multi-step chemical reactions, often involving protection and deprotection strategies to control the reactivity of the functional groups.

835-24-5

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835-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 835-24-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 835-24:
(5*8)+(4*3)+(3*5)+(2*2)+(1*4)=75
75 % 10 = 5
So 835-24-5 is a valid CAS Registry Number.

835-24-5Relevant academic research and scientific papers

An Au-Catalyzed Cyclialkylation of Electron-Rich Arenes with Epoxides to Prepare 3-Chromanols

Shi, Zhangjie,He, Chuan

, p. 5964 - 5965 (2004)

A gold-catalyzed cyclialkylation of electron-rich arenes with tethered epoxides afforded 3-chromanols stereospecifically. Copyright

NOVEL 1-PHENYLMONO- OR -POLYHYDROXYPROPANE COMPOUNDS, COMPOSITIONS AND COSMETIC USES THEREOF

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Page/Page column 28, (2017/04/04)

The present invention relates to novel compounds of formula (I) to compositions comprising same, and also to the use thereof for preventing and/or cosmetically treating the signs of aging of the skin.

Friedel-Crafts alkylation of arenes with epoxides promoted by fluorinated alcohols or water

Li, Guo-Xing,Qu, Jin

supporting information; experimental part, p. 2653 - 2655 (2010/07/08)

The stereoselective intra- and intermolecular Friedel-Crafts alkylation of electron-rich arenes with epoxides can take place in refluxing 1,1,1,3,3,3-hexafluoroisopropanol owing to its weak acidity and high ionizing power.

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