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Diethyl (4-methyl-3-oxo-1-phenylpentyl)propanedioate is a complex organic compound with the molecular formula C20H26O4. It is a derivative of diethyl propanedioate, featuring a 4-methyl-3-oxo-1-phenylpentyl group attached to the propanedioate backbone. diethyl (4-methyl-3-oxo-1-phenylpentyl)propanedioate is characterized by its ester functional groups and a ketone group within the 4-methyl-3-oxo-1-phenylpentyl moiety. It is likely to be used in the synthesis of various pharmaceuticals, fragrances, or other specialty chemicals due to its unique structure and reactivity. The compound's specific applications and properties would depend on its ability to participate in chemical reactions, such as esterification, reduction, or condensation, which could be exploited in the creation of more complex molecules.

5435-09-6

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5435-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5435-09-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5435-09:
(6*5)+(5*4)+(4*3)+(3*5)+(2*0)+(1*9)=86
86 % 10 = 6
So 5435-09-6 is a valid CAS Registry Number.

5435-09-6SDS

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-(4-methyl-3-oxo-1-phenylpentyl)propanedioate

1.2 Other means of identification

Product number -
Other names (4-Methyl-3-oxo-1-phenyl-pentyl)-malonsaeure-diaethylester

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:5435-09-6 SDS

5435-09-6Relevant academic research and scientific papers

A new and versatile route for the synthesis of highly substituted benzenoids

Robl, Jeffrey A.

, p. 3421 - 3424 (2007/10/02)

A new route for the synthesis of highly substituted benzenoids has been developed. Key steps include the conversion of unsaturated lactone 7 to carboxy substituted cyclohexenone 8 followed aromatization to give phenol 9. The phenolic functionality provides a handle for further modification to give substituted benzenoids of type 2.

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