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Methyl 2-[4-[2-[4-(methoxycarbonylmethyl)phenyl]ethyl]phenyl]acetate is a complex organic compound with the molecular formula C21H22O5. It is a derivative of acetic acid, featuring a methyl ester group attached to the acetate backbone. The molecule contains a phenyl ring with a methoxycarbonylmethyl substituent, which is a combination of a methoxy group and a carbonyl group attached to a methyl group. Additionally, it has a phenylethyl group, which is an ethyl group with a phenyl substituent, attached to another phenyl ring. methyl 2-[4-[2-[4-(methoxycarbonylmethyl)phenyl]ethyl]phenyl]acetate is characterized by its intricate structure, which includes multiple phenyl rings and a variety of functional groups, making it a potentially interesting candidate for further chemical or pharmaceutical research.

4253-33-2

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4253-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4253-33-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4253-33:
(6*4)+(5*2)+(4*5)+(3*3)+(2*3)+(1*3)=72
72 % 10 = 2
So 4253-33-2 is a valid CAS Registry Number.

4253-33-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[4-[2-[4-(2-methoxy-2-oxoethyl)phenyl]ethyl]phenyl]acetate

1.2 Other means of identification

Product number -
Other names Bibenzyl-4,4'-diyl-di-essigsaeure-dimethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:4253-33-2 SDS

4253-33-2Downstream Products

4253-33-2Relevant academic research and scientific papers

Syntheses d'amidoesters par reaction de Kolbe

Abderrahman, Ben Moufida,Laurent, Eliane,Marquet, Bernard

, p. 571 - 578 (2007/10/02)

The synthesis of amidoesters has been investigated by anodic cooxidation of diacid hemiesters CO2H-CH2-Z-CO2CH3 -CH2-> and amidoacids R1-N(Y)-(CH2)2-CO2H .The scope of this reaction was examined in detail.This synthetic pathway provided very a simple access to a wide range of amidoesters R1-N(Y)-(CH2)3-Z-CO2CH3 by varying Z and R1 as well as n value.

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