65466-10-6 Usage
Description
(Z)-pent-2-en-1-yl benzoate, also known as cis-2-penten-1-yl benzoate, is a chemical compound with the formula C13H14O2. It is a colorless to pale yellow liquid characterized by its sweet, fruity odor. (Z)-pent-2-en-1-yl benzoate is derived from the esterification of benzoic acid with (Z)-2-penten-1-ol and is valued for its pleasant aroma, which is often described as sweet, floral, and slightly fruity.
Uses
Used in Flavor and Fragrance Industry:
(Z)-pent-2-en-1-yl benzoate is used as a flavor and fragrance ingredient for its sweet, fruity scent and pleasant aroma. It is commonly added to perfumes, skincare products, and household cleaners to enhance their fragrance and appeal to consumers.
Used in Insect Control:
(Z)-pent-2-en-1-yl benzoate is used as a pheromone in the insect control industry. Its natural scent attracts specific insects, making it an effective tool for monitoring and managing insect populations.
Used in Food and Beverage Industry:
In the food and beverage industry, (Z)-pent-2-en-1-yl benzoate is used as a flavoring agent. Its sweet, fruity taste adds a pleasant flavor to various products, enhancing their overall taste and consumer experience.
Check Digit Verification of cas no
The CAS Registry Mumber 65466-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,6 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65466-10:
(7*6)+(6*5)+(5*4)+(4*6)+(3*6)+(2*1)+(1*0)=136
136 % 10 = 6
So 65466-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O2/c1-2-3-7-10-14-12(13)11-8-5-4-6-9-11/h3-9H,2,10H2,1H3/b7-3+
65466-10-6Relevant articles and documents
Wacker-type oxidation of internal alkenes using Pd(Quinox) and TBHP
Deluca, Ryan J.,Edwards, Jennifer L.,Steffens, Laura D.,Michel, Brian W.,Qiao, Xiaoxiao,Zhu, Chunyin,Cook, Silas P.,Sigman, Matthew S.
, p. 1682 - 1686 (2013/04/10)
The Pd-catalyzed TBHP-mediated Wacker-type oxidation of internal alkenes is reported. The reaction uses 2-(4,5-dihydro-2-oxazolyl)quinoline (Quinox) as ligand and TBHP(aq) as oxidant to deliver single ketone constitutional isomer products in a predictable fashion from electronically biased olefins. This methodology is showcased through its application on an advanced intermediate in the total synthesis of the antimalarial drug artemisinin.
Stereoselective Preparation of (E)-Allyl Alcohols via Radical Elimination from anti-γ-Phenylthio-β-nitro Alcohols
Kamimura, Akio,Ono, Noboru
, p. 1278 - 1280 (2007/10/02)
Phenylthio and hydroxymethyl groups may be introduced into nitroalkenes stereoselectively by treatment with benzenethiol and aqueous formaldehyde to give anti-γ-phenylthio-β-nitro alcohols, which are converted into (E)-allyl alcohols via radical elimination induced by Bu3SnH.