29474-19-9 Usage
General Description
Bicyclo[3.2.0]hept-6-en-3-one, also known as 3-norcarene-2-one, is a bicyclic compound with a ketone functional group. Its molecular structure consists of a seven-membered ring with a double bond and a carbonyl group at the C-3 position. Bicyclo[3.2.0]hept-6-en-3-one is commonly used in organic synthesis as a versatile building block for the preparation of various chemical compounds. It is also utilized as a starting material for the synthesis of natural products and biologically active compounds. Bicyclo[3.2.0]hept-6-en-3-one has been found to exhibit insecticidal and antifungal properties, making it a potential candidate for the development of new pest control agents.
Check Digit Verification of cas no
The CAS Registry Mumber 29474-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,7 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29474-19:
(7*2)+(6*9)+(5*4)+(4*7)+(3*4)+(2*1)+(1*9)=139
139 % 10 = 9
So 29474-19-9 is a valid CAS Registry Number.
29474-19-9Relevant articles and documents
ELECTRON TRANSFER PHOTOOXYGENATION OF 3,5-CYCLOHEPTADIENONES AND RELATED COMPOUNDS
Wilczak, Wojciech A.,Schuster, David I.
, p. 5331 - 5334 (1986)
3,5-Cycloheptadienones undergo electron transfer to photoexcited DCA in oxygen-free CH3CN solution to give triplet products which arise via back electron transfer form initially formed radical ion pairs.Photooxygenation of 2,2,7,7-tetramethyl-3,5-cycloheptadienone (1) and the derived methyl ether (4) under electron-transfer conditions results in unusual hydroperoxidederived products.The related alcohol (3)gives a product strongly suggestive of intramolecular capture by an OH group of a diene radical cation.
