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Diethyl 2-acetamido-2-[(3-methylphenyl)methyl]propanedioate is a complex organic compound with the chemical formula C20H27NO5. It is a derivative of propanedioic acid, featuring an acetamido group and a 3-methylphenylmethyl substituent. diethyl 2-acetamido-2-[(3-methylphenyl)methyl]propanedioate is characterized by its ester functional groups, which are derived from the reaction of propanedioic acid with ethanol. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and chemical intermediates. The compound's structure and properties make it a valuable building block in organic chemistry, particularly in the preparation of complex molecules with potential applications in the medical and chemical industries.

5440-54-0

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5440-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5440-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5440-54:
(6*5)+(5*4)+(4*4)+(3*0)+(2*5)+(1*4)=80
80 % 10 = 0
So 5440-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO5/c1-5-22-15(20)17(18-13(4)19,16(21)23-6-2)11-14-9-7-8-12(3)10-14/h7-10H,5-6,11H2,1-4H3,(H,18,19)

5440-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-acetamido-2-[(3-methylphenyl)methyl]propanedioate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5440-54-0 SDS

5440-54-0Relevant academic research and scientific papers

Organocatalytic Enantioselective Addition of α-Aminoalkyl Radicals to Isoquinolines

Liu, Xiangyuan,Liu, Yang,Chai, Guobi,Qiao, Baokun,Zhao, Xiaowei,Jiang, Zhiyong

, p. 6298 - 6301 (2018/10/09)

With a dual organocatalytic system involving a chiral phosphoric acid and a dicyanopyrazine-derived chromophore (DPZ) photosensitizer and under the irradiation with visible light, an enantioselective Minisci-type addition of α-amino acid-derived redox-active esters (RAEs) to isoquinolines has been developed. A variety of prochiral α-aminoalkyl radicals generated from RAEs were successfully introduced on isoquinolines, providing a range of valuable α-isoquinoline-substituted chiral secondary amines in high yields with good to excellent enantioselectivities.

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