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41891-38-7

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41891-38-7 Usage

General Description

Ethyl 3-methyl-4-oxo-2-butenoate, also known as ethyl acetoacetate, is an organic compound with the molecular formula C6H10O3. It is a colorless liquid with a fruity odor, commonly used as a flavoring agent and in the production of pharmaceuticals and perfumes. Ethyl acetoacetate is also used as a precursor in the synthesis of various compounds, including pharmaceuticals, dyes, and polymers. It is often employed as a reagent in organic chemistry reactions, particularly in the formation of beta-keto esters, which are useful intermediates in the synthesis of many complex organic molecules. Ethyl acetoacetate is a versatile chemical compound with a wide range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 41891-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,9 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41891-38:
(7*4)+(6*1)+(5*8)+(4*9)+(3*1)+(2*3)+(1*8)=127
127 % 10 = 7
So 41891-38-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O3/c1-3-10-7(9)4-6(2)5-8/h4-5H,3H2,1-2H3/b6-4+

41891-38-7SDS

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 (E)-ethyl 3-methyl-4-oxobut-2-enoate

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:41891-38-7 SDS

41891-38-7Relevant articles and documents

Anomalous Reactivity and Selectivity in the Intermolecular Diels-Alder Reactions of Multisubstituted Acyclic Dienes with Geometrical Isomers of Enals

Zhou, Jia-Hui,Cai, Sai-Hu,Xu, Yun-He,Loh, Teck-Peng

supporting information, p. 2355 - 2358 (2016/06/09)

A Lewis-acid catalyzed intermolecular Diels-Alder reaction between multisubstituted acyclic dienes and the E and Z isomers of α,β-enals was studied. It was found that the diene reacted selectively with the Z-isomer of the α,β-enal.

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