10035-96-8 Usage
General Description
(E)-3-Cyclodecen-1-one, also known as 3-cyclodecen-1-one, is a chemical compound that belongs to the class of cyclic ketones. It is a colorless liquid with a slightly sweet, floral odor. It is primarily used as a flavoring agent in the food and beverage industry, imparting a sweet, fruity, and floral note to various products. It is also utilized in the production of perfumes and as a fragrance ingredient in personal care products. Additionally, (E)-3-Cyclodecen-1-one has been studied for its potential pharmacological and medicinal properties, including its anti-inflammatory and antifungal activities. Overall, (E)-3-Cyclodecen-1-one plays a crucial role in the flavor, fragrance, and pharmaceutical industries due to its unique sensory and biological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 10035-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10035-96:
(7*1)+(6*0)+(5*0)+(4*3)+(3*5)+(2*9)+(1*6)=58
58 % 10 = 8
So 10035-96-8 is a valid CAS Registry Number.
10035-96-8Relevant articles and documents
Synthetic Applications in Radical/Radical Cationic Cascade Reactions
Rinderhagen, Heiko,Mattay, Jochen
, p. 851 - 874 (2007/10/03)
Oxidative photoinduced electron transfer (PET) reactions have been performed with various cyclic cyclopropyl(vinyl) silyl ethers bearing an olefinic or acetylenic side chain. The reactions result in bi- to tetracyclic ring systems via a fragmentation-radical/radical cationic addition reaction pathway with well defined ring juncture. The mode of cyclisation (endo/exo) can be partially controlled by addition of nucleophiles due to the suppression of radical cationic reaction pathways. Quantum chemical calculation of the cyclisation transition states underline the experimentally found selectivities. Additional mechanistic studies concerning the saturation step reveal that the final radical is saturated mostly by the solvent and traces of water in the solvent.