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4-Decenoic acid methyl ester, also known as methyl 4-decenoate, is a chemical compound with the molecular formula C11H20O2. It is an ester derived from 4-decenoic acid, which is a monounsaturated fatty acid with a double bond between the 4th and 5th carbon atoms. 4-Decenoic acid methyl ester is characterized by its fruity, green, and slightly fatty odor, and it is commonly used in the flavor and fragrance industry to impart a natural, fresh, and fruity scent to various products. It can be found in trace amounts in some fruits, such as passion fruit and mango, and is also used as a synthetic flavoring agent in food and beverages. Due to its chemical structure, 4-decenoic acid methyl ester is known for its potential antimicrobial properties and is being studied for its potential applications in various industries.

1191-02-2

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1191-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1191-02-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1191-02:
(6*1)+(5*1)+(4*9)+(3*1)+(2*0)+(1*2)=52
52 % 10 = 2
So 1191-02-2 is a valid CAS Registry Number.

1191-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl dec-4-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

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More Details:1191-02-2 SDS

1191-02-2Upstream product

1191-02-2Relevant articles and documents

A convenient triisobutylaluminium (TIBAL)-promoted Johnson-Claisen approach to γ,δ-unsaturated alcohols

Cosgrove, Kelly L.,McGeary, Ross P.

experimental part, p. 1749 - 1752 (2009/12/04)

Mixed ortho esters derived from allylic alcohols undergo methanol elimination in the presence of triisobutylaluminium (TIBAL) at room temperature to form mixed ketene acetals. TIBAL then promotes immediate Claisen rearrangement of these intermediates, and

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