32960-67-1 Usage
General Description
(1E)-1-(4-methoxyphenyl)cyclooctene is a chemical compound with the molecular formula C15H18O. It is classified as a cycloalkene, which is a type of unsaturated hydrocarbon with a ring structure containing at least one double bond. The presence of the 4-methoxyphenyl group indicates that this compound contains a benzene ring with a methoxy (-OCH3) functional group attached at the para position. This chemical is often used in organic synthesis and medicinal chemistry research due to its versatile reactivity and potential biological activity. Its unique structure and properties make it a valuable building block for the creation of new compounds with various applications in the pharmaceutical and agrochemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 32960-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 32960-67:
(7*3)+(6*2)+(5*9)+(4*6)+(3*0)+(2*6)+(1*7)=121
121 % 10 = 1
So 32960-67-1 is a valid CAS Registry Number.
32960-67-1Relevant articles and documents
Application of a readily available and air stable monophosphine HBF4 salt for the Suzuki coupling reaction of aryl or 1-alkenyl chlorides
Lü, Bo,Fu, Chunling,Ma, Shengming
supporting information; experimental part, p. 1284 - 1286 (2010/04/27)
In this Letter, a readily available monophosphine HBF4 salt was applied for the Suzuki coupling reactions of organoboronic acids to afford the cross-coupling products in high to excellent yields. Both aryl or 1-alkenyl boronic acids and chlorides may be used. It is also suitable for sterically hindered cases.
Ni(O) catalyzed reactions of aryl and vinyl halides with alkenes and alkynes
Iyer, Suresh,Ramesh, Chinnasamy,Ramani
, p. 8533 - 8536 (2007/10/03)
NI[P(OPh)3]4 and Ni[P(OET)3]4 catalyze the reaction of aryl and vinyl halides with olefins (Heck reaction) and alkynes.
Process for the manufacture of new carboxylic acids
-
, (2008/06/13)
α-Phenoxyacetic acids, in which the α-position is substituted by an alkyl residue with 5 to 12 carbon atoms and the phenyl residue is substituted by a cycloaliphatic hydrocarbon residue which is unsaturated in the 1-position and is only singly unsaturated
