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2-Ethyl-3-oxo-N-phenylhexanamide is a chemical compound with the molecular formula C15H19NO2. It is a derivative of hexanamide, featuring a phenyl group attached to the nitrogen atom, an ethyl group at the 2nd carbon, and a ketone group at the 3rd carbon. 2-ethyl-3-oxo-N-phenylhexanamide is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs. Its structure and properties make it a versatile building block for the development of new therapeutic agents.

5659-19-8

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5659-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5659-19-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5659-19:
(6*5)+(5*6)+(4*5)+(3*9)+(2*1)+(1*9)=118
118 % 10 = 8
So 5659-19-8 is a valid CAS Registry Number.

5659-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-3-oxo-N-phenylhexanamide

1.2 Other means of identification

Product number -
Other names 2-Aethyl-3-oxo-hexansaeure-anilid

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5659-19-8 SDS

5659-19-8Downstream Products

5659-19-8Relevant academic research and scientific papers

Aerobic α-hydroxylation of β-keto esters and amides by co-catalysis of SmI3 and I2 under mild base-free conditions

Yu, Shun-Ming,Cui, Kai,Lv, Fei,Yang, Zhen-Yu,Yao, Zhu-Jun

supporting information, p. 2818 - 2821 (2016/06/09)

A clean base-free α-hydroxylation of β-keto esters and amides has been developed, in which air was used as the oxygen source and SmI3 and I2 were applied as the catalysts, affording the corresponding α-hydroxylated 1,3-dicarbonyl pro

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