41114-00-5 Usage
Description
N-PENTADECANOIC ACID ETHYL ESTER, also known as Ethyl Pentadecanoate, is an organic compound with the chemical formula C17H34O2. It is a colorless to pale yellow liquid with a mild, fruity odor. Ethyl Pentadecanoate is commonly found in cork stoppers produced by fungi and is used in various applications due to its unique properties.
Uses
Used in Flavor and Fragrance Industry:
Ethyl Pentadecanoate is used as a flavor compound for enhancing the taste and aroma of various food products. Its mild, fruity odor makes it a suitable additive for the creation of artificial fruit flavors, particularly in the context of the food and beverage industry.
Used in Cork Stopper Production:
Ethyl Pentadecanoic Acid Ethyl Ester is used as an off-flavor compound in the production of cork stoppers. The presence of this compound in cork stoppers can sometimes lead to an undesirable taste in bottled beverages, which is why its levels are monitored and controlled during the manufacturing process.
Check Digit Verification of cas no
The CAS Registry Mumber 41114-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,1 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41114-00:
(7*4)+(6*1)+(5*1)+(4*1)+(3*4)+(2*0)+(1*0)=55
55 % 10 = 5
So 41114-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H34O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-4-2/h3-16H2,1-2H3
41114-00-5Relevant articles and documents
Iron-catalyzed AlkylAlkyl negishi coupling of organoaluminum reagents
Agata, Ryosuke,Kawamura, Shintaro,Isozaki, Katsuhiro,Nakamura, Masaharu
supporting information, p. 238 - 241 (2019/03/13)
The first iron-catalyzed cross-coupling reaction of alkyl halides with alkylaluminum reagents (alkylalkyl Negishi coupling) is developed using an iron/bisphosphine catalyst system. The reaction shows high functional group tolerance: various primary alkyl halides possessing a non-protected indole, carboxyl, or hydroxy group are coupled with primary alkylaluminum reagents in good yields. Potassium fluoride plays a key role to promote the reaction by generating an aluminate species, which facilitates the transmetalation between the organoaluminum and the iron catalyst.
Selective Mono- and Bis(alkoxycarbonylation)s of Olefins Catalyzed by Palladium in the Presence of Cu(I) or Cu(II) Chloride under Remarkably Mild Conditions. Application to the Synthesis of γ-Butyrolactone Derivatives
Toda, Shiho,Miyamoto, Masanori,Kinoshita, Hideki,Inomata, Katsuhiko
, p. 3600 - 3606 (2007/10/02)
Palladium-catalyzed mono- and bis(alkoxycarbonylation)s of the olefins were controlled by the use of copper(II) and copper(I) chloride, respectively, in alcohol under normal pressure of carbon monoxide and oxygen at room temperature without any other additives. 3-Buten-1-ols gave the corresponding γ-butyrolactones and 2-oxotetrahydrofuran-3-acetic acid esters, respectively, in high yields.
