79218-15-8 Usage
Uses
Used in the Food and Beverage Industry:
TERT-BUTYL CROTONATE is used as a flavoring agent for its distinctive fruity scent, enhancing the taste and aroma of various food and drink products.
Used in the Fragrance Industry:
TERT-BUTYL CROTONATE is used as a raw material in the synthesis of fragrances, contributing to the creation of diverse scent profiles for use in perfumes, cosmetics, and other scented products.
Used in the Chemical Synthesis Industry:
TERT-BUTYL CROTONATE is utilized as a starting material for the synthesis of other organic compounds, taking advantage of its stable and low reactive properties to produce a variety of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 79218-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,1 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79218-15:
(7*7)+(6*9)+(5*2)+(4*1)+(3*8)+(2*1)+(1*5)=148
148 % 10 = 8
So 79218-15-8 is a valid CAS Registry Number.
79218-15-8Relevant academic research and scientific papers
One-pot ester synthesis from allyl and benzyl halides and alcohols by palladium-catalyzed carbonylation
Tommasi, Sara,Perrone, Serena,Rosato, Francesca,Salomone, Antonio,Troisi, Luiginio
experimental part, p. 423 - 430 (2012/03/11)
A mild and efficient one-pot synthesis of esters based on the Pd-catalyzed alkoxy- and aryloxycarbonylation of allylic and benzylic halides is described. The methodology has been applied to primary, secondary, and tertiary alcohols as well as to phenol derivatives. The O-protection of some biologically relevant molecules is also reported. Georg Thieme Verlag Stuttgart New York.
A VERSATILE ROUTE TO MIXED VINYLKETENE ACETALS : USE OF 1-t-BUTYLDIMETHYLSILOXY-1-ETHOXY BUTADIENE IN CYCLOHEXENONE SYNTHESIS
Lombardo, Luciano
, p. 381 - 384 (2007/10/02)
The successful entry to the diverse mixed vinylketene acetals 3 extends the participation of these intermediates in cyclohexenone synthesis.
