759-54-6 Usage
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.
Uses
Used in Food and Beverage Industry:
Ethyl 2-cyano-3-methylhex-2-enoate is used as a flavoring agent for imparting a fruity aroma and taste to various food and beverage products.
Used in Pharmaceutical Industry:
Ethyl 2-cyano-3-methylhex-2-enoate is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agricultural Industry:
Ethyl 2-cyano-3-methylhex-2-enoate is used in the synthesis of agricultural products, such as pesticides and fertilizers, to enhance crop yield and protect plants from pests.
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+
759-54-6Relevant 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.
