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759-54-6

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759-54-6 Usage

General Description

Ethyl 2-cyano-3-methylhex-2-enoate is a chemical compound with the molecular formula C9H13NO2. It is a colorless liquid with a fruity odor, commonly used as a flavoring agent in the food and beverage industry. This chemical is also utilized in the synthesis of pharmaceuticals and agricultural products. Ethyl 2-cyano-3-methylhex-2-enoate is known for its mild irritant properties and should be handled with caution. It is important to carefully follow safety guidelines and regulations when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 759-54-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 759-54:
(5*7)+(4*5)+(3*9)+(2*5)+(1*4)=96
96 % 10 = 6
So 759-54-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-4-6-8(3)9(7-11)10(12)13-5-2/h4-6H2,1-3H3/b9-8+

759-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-cyano-3-methylhex-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Cyano-3-methyl-2-hexenoic acid ethyl ester

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:759-54-6 SDS

759-54-6Relevant articles and documents

Geminate-Substituted Cyclopentadienes. 1. Synthesis of 5,5-Dialkylcyclopentadienes via 4,4-Dialkylcyclopent-2-en-1-ones.

Holder, Richard W.,Daub, John P.,Baker, Wesley E.,Gilbert, Raymond H,Graf, Norman A.

, p. 1445 - 1451 (2007/10/02)

A synthetic route for the preparation of 5,5,-dialkylcyclopentadienes (1) via 4,4-dialkylcyclopent-2-en-1-ones (3) is described.Beginnig with ketones (in which the two carbonyl substituents will become the two alkyl groups in the title compounds), the route traverses the Guareschi imides 5, 3,3-dialkylglutaric acids 4 and their ethyl esters 7, masked acyloins 8, cyclopentenones 3, alkohols 9, and bromides 10 to reach the dienes 1.Physical properties of five such derivates 1 and 3 (dimethyl, methylethyl,diethyl, methyl-n-propyl, and methylisopropyl) are presented.

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