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Ethyl 4-oxo-3-(phenylcarbamoyl)pentanoate is a chemical compound with the molecular formula C14H17NO4. It is a derivative of pentanoic acid, featuring a phenylcarbamoyl group attached to the third carbon and an ester group at the fourth carbon. ethyl 4-oxo-3-(phenylcarbamoyl)pentanoate is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds. It is characterized by its ability to form an amide bond with phenylcarboxylic acid, which can be crucial in the creation of various drug molecules. The compound's structure allows for further functionalization and modification, making it a valuable intermediate in organic synthesis.

6331-47-1

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6331-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6331-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6331-47:
(6*6)+(5*3)+(4*3)+(3*1)+(2*4)+(1*7)=81
81 % 10 = 1
So 6331-47-1 is a valid CAS Registry Number.

6331-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-oxo-3-(phenylcarbamoyl)pentanoate

1.2 Other means of identification

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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

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More Details:6331-47-1 SDS

6331-47-1Relevant academic research and scientific papers

A Formal [3+2] Annulation of β-Oxoamides and 3-Alkyl- or 3-Aryl-Substituted Prop-2-Ynyl Sulfonium Salts: Substrate-Controlled Chemoselective Synthesis of Substituted γ-Lactams and Furans

Deng, Bicheng,Rao, Chitturi Bhujanga,Zhang, Rui,Li, Jiacheng,Liang, Yongjiu,Zhao, Yanning,Gao, Ming,Dong, Dewen

, p. 4549 - 4557 (2019/08/30)

A substrate-controlled synthesis of substituted γ-lactams and furans has been developed via a formal [3+2] annulation of β-oxoamides and 3-alkyl/arylprop-2-ynyl sulfonium salts in the presence of cesium carbonate in a chemoselective manner. This novel pro

A facile and efficient synthesis of polyfunctionalized pyridin-2(1H)-ones from β-oxo amides under Vilsmeier conditions

Xiang, Dexuan,Wang, Kewei,Liang, Yongjiu,Zhou, Guangyuan,Dong, Dewen

, p. 345 - 348 (2008/09/19)

(Chemical Equation Presented) A facile and efficient one-pot synthesis of polysubstituted pyridin-2(1H)-ones from a variety of β-oxo amides under Vilsmeier conditions is described, and a mechanism involving sequential halogenation, formylation and intramo

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