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N-(3-oxo-3-phenylpropyl)hexanamide is a chemical compound with the molecular formula C17H21NO2. It is a derivative of hexanamide, where the hexyl group is substituted with a 3-oxo-3-phenylpropyl group. N-(3-oxo-3-phenylpropyl)hexanamide is characterized by the presence of a ketone group (C=O) in the 3-position of the phenylpropyl moiety, which is connected to the hexanamide backbone through an amide linkage. The structure of N-(3-oxo-3-phenylpropyl)hexanamide features a phenyl ring, which contributes to its aromatic properties, and a hexyl chain, which provides a linear aliphatic character. The compound may have potential applications in the fields of pharmaceuticals, materials science, or as an intermediate in organic synthesis, although specific uses would depend on its physical and chemical properties, which are not detailed in this summary.

5431-40-3

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5431-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5431-40-3 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 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5431-40:
(6*5)+(5*4)+(4*3)+(3*1)+(2*4)+(1*0)=73
73 % 10 = 3
So 5431-40-3 is a valid CAS Registry Number.

5431-40-3SDS

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 1-phenyl-3-[4-(3-phenyl-propyl)-piperidin-1-yl]-propan-1-one

1.2 Other means of identification

Product number -
Other names N-(3-Oxo-3-phenyl-propyl)-hexanamid

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:5431-40-3 SDS

5431-40-3Downstream Products

5431-40-3Relevant academic research and scientific papers

Palladium-catalyzed synthesis of aryl ketones from boronic acids and carboxylic acids activated in situ by pivalic anhydride

Goossen, Lukas J.,Ghosh, Keya

, p. 3254 - 3267 (2007/10/03)

A new palladium-catalyzed cross-coupling reaction between arylboronic acids and mixed anhydrides, generated in situ from carboxylic acids and pivalic anhydride, is presented. Optimization of the new catalyst and the reaction conditions led to the development of a convenient one-pot ketone synthesis directly from carboxylic and boronic acids in the presence of different (phosphane)palladium complexes in wet THF at 60 °C. Systematic studies were performed to elucidate the reaction mechanism of this transformation. The scope and the limitations of the new process are demonstrated by the synthesis of 33 functionalized ketones. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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