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4-Pentenoic acid, 3-methyl, ethyl ester, also known as ethyl 3-methyl-4-pentenoate, is an organic compound with the chemical formula C7H12O2. It is a colorless liquid with a fruity, apple-like odor. This ester is formed by the reaction of 3-methyl-4-pentenoic acid with ethanol, resulting in the esterification process. It is commonly used as a flavoring agent and fragrance compound in the food and perfume industries due to its pleasant aroma. The compound is also known for its potential applications in the synthesis of various chemicals and pharmaceuticals. It is important to handle this substance with care, as it can cause skin and eye irritation, and it is considered a hazardous material.

7796-71-6

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7796-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7796-71-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7796-71:
(6*7)+(5*7)+(4*9)+(3*6)+(2*7)+(1*1)=146
146 % 10 = 6
So 7796-71-6 is a valid CAS Registry Number.

7796-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-methylpent-4-enoate

1.2 Other means of identification

Product number -
Other names 3-Methyl-pent-4-ensaeure-aethylester

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:7796-71-6 SDS

7796-71-6Relevant academic research and scientific papers

PREPARATION D'ESTERS γ-ETHYLENIQUES PAR ALLYLATION DU REACTIF DE REFORMATSKY EN PRESENCE DE SELS DE CUIVRE

Gaudemar, M.

, p. 2749 - 2752 (2007/10/02)

The Reformatsky organozinc compounds react easily with allylic halides in the presence of copper salts.The reaction is stereoselective and can be made regioselective with a proper choice of reaction conditions.

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