14925-75-8 Usage
Description
(2-prop-2-enylphenyl) prop-2-enoate, also known as cinnamyl cinnamate, is a chemical compound that belongs to the cinnamate ester family and is commonly found in plants such as cinnamon. It is known for its sweet, spicy aroma and is frequently used in the fragrance industry. Moreover, it has potential applications in the pharmaceutical and food industries due to its reported antimicrobial and antioxidant properties.
Uses
Used in Fragrance Industry:
(2-prop-2-enylphenyl) prop-2-enoate is used as a fragrance ingredient for its sweet, spicy aroma in the production of perfumes, lotions, and other scented products.
Used in Pharmaceutical Industry:
(2-prop-2-enylphenyl) prop-2-enoate is used as an antimicrobial and antioxidant agent in the development of pharmaceutical products.
Used in Food Industry:
(2-prop-2-enylphenyl) prop-2-enoate is used as a natural preservative and antibacterial agent in food and beverages to enhance their shelf life and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 14925-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,2 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14925-75:
(7*1)+(6*4)+(5*9)+(4*2)+(3*5)+(2*7)+(1*5)=118
118 % 10 = 8
So 14925-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O2/c1-3-7-10-8-5-6-9-11(10)14-12(13)4-2/h3-6,8-9H,1-2,7H2
14925-75-8Relevant articles and documents
Ruthenium carbene complexes with N,N'-bis(mesityl)imidazol-2-ylidene ligands: RCM catalysts of extended scope
Fuerstner, Alois,Thiel, Oliver R.,Ackermann, Lutz,Schanz, Hans-Joerg,Nolan, Steven P.
, p. 2204 - 2207 (2007/10/03)
The ruthenium carbene complexes 3a,b bearing imidazol-2-ylidene ligands constitute excellent precatalysts for ring-closing metathesis (RCM) reactions allowing the formation of tri- and tetrasubstituted cycloalkenes. They also apply to annulations that are beyond the scope of the standard Grubbs carbene 1 as well as to ring-closing reactions of acrylic acid derivatives even if the resulting α,β-unsaturated lactones (or lactams) are tri- or tetrasubstituted. The reactivity of 3a was found to be highly dependent on the reaction medium: particularly high reaction rates are observed in toluene, although this solvent also leads to an increased tendency of the catalyst to isomerize the double bonds of the substrates.
