65466-10-6 Usage
General 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 with a sweet, fruity odor. (Z)-pent-2-en-1-yl benzoate is commonly used as a flavor and fragrance ingredient in a variety of products, such as perfumes, skincare products, and household cleaners. It is derived from the esterification of benzoic acid with (Z)-2-penten-1-ol. (Z)-Pent-2-en-1-yl benzoate is known for its pleasant aroma, which is often described as sweet, floral, and slightly fruity. It is also used as a pheromone in insect control and has applications in the food and beverage industry as a flavoring agent.
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.
