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1-acetyl-4-{1-methyl-1-(4-acetyloxyphenyl)ethyl}benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1256572-99-2

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1256572-99-2 Usage

Molecular Weight

312.37 g/mol

Structure

A complex molecular structure containing a benzene ring substituted with an acetyl group and a methyl group attached to a phenethyl moiety, which in turn is attached to another phenyl group with an acetyloxy substitution.

Functional Groups

Acetyl (-COCH3), Methyl (-CH3), Phenyl (C6H5), and Acetyloxy (-OCOCH3) groups.

Appearance

Likely a solid or oily liquid due to its molecular weight and complexity.

Solubility

Soluble in organic solvents such as dichloromethane, acetone, and ethanol, but may have limited solubility in water.

Stability

Stable under normal temperature and pressure conditions, but sensitive to heat, light, and moisture.

Reactivity

Reactive towards nucleophiles and electrophiles due to the presence of acetyl and acetyloxy groups.

Applications

Used in the field of organic chemistry for various synthetic reactions and may have potential applications in the pharmaceutical industry.

Research and Experimentation

Its unique structure and functional groups make it a versatile compound for the development of new drugs and materials, and a valuable tool for research and experimentation in the lab.

Check Digit Verification of cas no

The CAS Registry Mumber 1256572-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,5,7 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1256572-99:
(9*1)+(8*2)+(7*5)+(6*6)+(5*5)+(4*7)+(3*2)+(2*9)+(1*9)=182
182 % 10 = 2
So 1256572-99-2 is a valid CAS Registry Number.

1256572-99-2Relevant academic research and scientific papers

Method for catalytically synthesizing 4-acylarylalkylphenol derivative

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Page/Page column 4-8, (2019/10/01)

The present invention discloses a method for catalytically synthesizing a 4-acylarylalkylphenol derivative. P-cumylphenol reacts with an acylating agent under the catalysis of a modified attapulgite solid acid to generate the 4-acylaralkylphenol derivativ

METHOD FOR PRODUCING TRISPHENOLS AND MONOESTER-SUBSTITUTED PRODUCTS THEREOF, AND 4-ACYLARALKYLPHENOL DERIVATIVES

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Page/Page column 16, (2012/05/07)

Trisphenols of general formula (1), which are useful as starting materials for polymer, are industrially easily produced by a method using as a starting material 4-aralkylphenol derivatives expressed by general formula (2): wherein X represents a hydrogen atom or leaving group that can be substituted with a hydrogen atom.

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